(14 days)
Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows: General, OB, Gynecology, Abdomen, Fetal Heart, Renal, Neonatal, Pediatric, Vascular, Cardiac, Urology, Breast, Small Parts, Musculoskeletal applications. The system also provides for the measurement of anatomical structures and for analysis packages that provide information that is used for clinical diagnosis purposes.
The SONOACE PICO is a general purpose, mobile, software controlled, diagnostic ultrasound system with on-screen display for themal and mechanical indices related to potential bioeffect mechanisms. Its function is to acquire ultrasound data and to display the data as B-mode, M-mode, Color Doppler, Pulsed (PW) Doppler, Power Doppler, Harmonic imaging and 3D imaging , or as a combination of these modes on the LCD monitor.
The provided document is a 510(k) summary for the SONOACE PICO Diagnostic Ultrasound System, dated May 16, 2006. This type of document is primarily concerned with establishing substantial equivalence to a predicate device, rather than presenting a detailed clinical study demonstrating the device's performance against specific acceptance criteria.
The information provided outlines the device's intended use and technological characteristics, and relies on its similarity to previously cleared devices (K013627, SA8000 Ultrasound system and K043455, SA8000 SE Ultrasound system) to demonstrate safety and effectiveness. It does not include a description of a specific study to prove that the device meets defined acceptance criteria in terms of diagnostic performance (e.g., sensitivity, specificity for a particular clinical condition). Instead, it lists the product safety standards it has been designed to meet.
Therefore, many of the requested sections (e.g., table of acceptance criteria and reported device performance, sample size for test set, number of experts, adjudication method, MRMC study, standalone performance, ground truth types, training set sample size, and ground truth establishment for training set) cannot be extracted from this document as they are not typically part of a 510(k) summary focused on substantial equivalence for a diagnostic ultrasound system.
However, I can extract the safety acceptance criteria mentioned:
1. Table of Acceptance Criteria and Reported Device Performance
This document focuses on compliance with general safety and performance standards for diagnostic ultrasound equipment, rather than specific clinical performance metrics. The "reported device performance" in this context refers to the device being designed to meet these standards.
| Acceptance Criteria (Safety/Technical Standards) | Reported Device Performance (Compliance) |
|---|---|
| UL 60601-1, Safety requirements for Medical Equipment | Designed to meet |
| CSA C22.2 No. 601.1, Safety requirements for Medical Equipment | Designed to meet |
| IEC60601-2-37, Diagnostic Ultrasound Safety Standards | Designed to meet |
| EN/IEC60601-1, Safety requirements for Medical Equipment | Designed to meet |
| EN/IEC60601-1-2, EMC requirements for Medical Equipment | Designed to meet |
| NEMA UD 2-2004 Acoustic Output Measurement Standard for Diagnostic Ultrasound Equipment | Designed to meet |
| NEMA UD 3-2004 Standard for Real Time Display of Thermal and Mechanical Acoustic Output Indices on Diagnostic Ultrasound Equipment | Designed to meet |
| IEC 61157, Declaration of the acoustic output | Designed to meet |
| ISO10993, Biocompatibility | Designed to meet |
The specific "study that proves the device meets the acceptance criteria" is not detailed in this 510(k) summary. For devices cleared through the 510(k) process, especially for ultrasound systems, substantial equivalence to a predicate device often serves as the basis for demonstrating safety and effectiveness, rather than new extensive clinical performance studies. The document states that "The SONOACE PICO is substantially equivalent to the SA8000 Diagnostic Ultrasound System, cleared via K013627, and the SA8000 SE Diagnostic Ultrasound System, cleared via K043455." This implies that the previous clearance of these predicate devices, based on their safety and performance data, is sufficient to demonstrate the new device's compliance.
A post-clearance special report is required for acoustic output measurements based on production line devices (Appendix G, "Information for Manufacturers Seeking Marketing Clearance of Diagnostic Ultrasound Systems and Transducers"), which is a verification step of manufacturing compliance rather than a clinical performance study.
The following information cannot be extracted from the provided document as it relates to clinical performance studies which are not typically required for 510(k) clearance of these types of devices based on substantial equivalence:
- Sample size used for the test set and the data provenance (e.g. country of origin of the data, retrospective or prospective): Not provided.
- Number of experts used to establish the ground truth for the test set and the qualifications of those experts (e.g. radiologist with 10 years of experience): Not provided.
- Adjudication method (e.g. 2+1, 3+1, none) for the test set: Not provided.
- If a multi reader multi case (MRMC) comparative effectiveness study was done, If so, what was the effect size of how much human readers improve with AI vs without AI assistance: Not provided (this is not an AI device).
- If a standalone (i.e. algorithm only without human-in-the-loop performance) was done: Not applicable (this is an ultrasound imaging system, not an algorithm for diagnosis).
- The type of ground truth used (expert consensus, pathology, outcomes data, etc): Not provided.
- The sample size for the training set: Not applicable (this is a hardware/software system, no AI training specified).
- How the ground truth for the training set was established: Not applicable.
{0}------------------------------------------------
SONOACE PICO Diagnostic
MAY 16 2006
510(K) SUMMARY OF SAFETY AND EFFECTIVENESS
This summary of safety and effectiveness is provided as part of this Premarket Notification in compliance with 21 CFR, Part 807, Subpart E, Section 807.92.
1. Submitter's Information: 21 CFR 807.92(a)(1)
Medison Co. Ltd. 1003, Daechi-dong, Gangnam-gu, Seoul 135-280, Korea
Contact Person: Mr. Kyung-Am, Shim Regulatory Affairs Manager
| Telephone: | 82.2.2194.1381 |
|---|---|
| Facsimile: | 82.2.2194.1399 |
| Email: | kashim@medison.com |
Data Prepared: April 10, 2006
2. Name of the device:
Common/Usual Name:
Diagnostic Ultrasound System and Accessories
Proprietary Name:
SONOACE PICO Diagnostic Ultrasound System
| Classification Names: | FR Number | Product Code |
|---|---|---|
| Ultrasonic Pulsed Doppler Imaging System | 892.1550 | 90-IYN |
| Ultrasound Pulsed Echo Imaging System | 892.1560 | 90-IYO |
| Diagnostic Ultrasound Transducer | 892.1570 | 90-ITX |
3. Identification of the predicate or legally marketed device:
K013627, 11/16/2001, SA8000 Ultrasound system K043455, 12/21/2004, SA8000 SE Ultrasound system
. .. ..
4. Device Description:
The SONOACE PICO is a general purpose, mobile, software controlled, diagnostic ultrasound system with on-screen display for themal and mechanical indices related to potential bioeffect mechanisms. Its function is to acquire ultrasound data and to display the data as B-mode, M-mode, Color Doppler, Pulsed (PW) Doppler, Power Doppler, Harmonic imaging and 3D imaging , or as a combination of these modes on the LCD monitor.
510(k) Summary of Safety and Effectiveness
ATTACHMENT 1(b)
{1}------------------------------------------------
The SONOACE PICO has been designed to meet the following product safety standards:
- UL 60601-1, Safety requirements for Medical Equipment -
- -CSA C22.2 No. 601.1, Safety requirements for Medical Equipment
- -IEC60601-2-37, Diagnostic Ultrasound Safety Standards
- EN/IEC60601-1, Safety requirements for Medical Equipment -
- EN/IEC60601-1-2, EMC requirements for Medical Equipment y -
- -NEMA UD 2-2004 Acoustic Output Measurement Standard for Diagnostic Ultrasound Equipment
- -NEMA UD 3-2004 Standard for Real Time Display of Thermal and Mechanical Acoustic Output Indices on Diagnostic Ultrasound Equipment
- IEC 61157, Declaration of the acoustic output .
- -ISO10993, Biocompatibility
5. Intended Uses:
The SONOACE PICO system is intended for the following applications: General, OB, Gynecology, Abdomen, Fetal Heart, Renal, Neonatal, Pediatric, Vascular, Cardiac, Urology, Breast, Small Parts, Musculoskeletal applications.
The system also provides for the measurement of anatomical structures and for analysis packages that provide information that is used for clinical diagnosis purposes.
6. Technological Characteristics:
The SONOACE PICO is substantially equivalent to the SA8000 Diagnostic Ultrasound System, cleared via K013627, and the SA8000 SE Diagnostic Ultrasound System, cleared via K043455. All systems transmit ultrasonic energy into patients, then perform post processing of received echoes to generate on-screen display of anatomic structures and fluid flow within the body. All system allow for specialized measurements of structures and flow, and calculations.
END of 510(K) Summary
510(k) Summary of Safety and Effectiveness
.. .. . . . . .
ATTACHMENT 1(b)
{2}------------------------------------------------
Image /page/2/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of a stylized caduceus symbol, which is a staff with two snakes coiled around it, and the text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" arranged in a circular fashion around the symbol. The text is in all caps and is evenly spaced around the circle.
Public Health Service
Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850
MAY 1 6 2006
Medison Co., Ltd. % Mr. Mark Job Responsible Third Party Official Regulatory Technology Services LLC 1394 25th Street NW BUFFALO MN 55313
Re: K061213
Trade Name: SONOACE PICO Ultrasound System Regulation Number: 21 CFR 892.1550 Regulation Name: Ultrasonic pulsed doppler imaging system Regulation Number: 21 CFR 892.1560 Regulation Name: Ultrasonic pulsed echo imaging system Regulation Number: 21 CFR 892.1570 Regulation Name: Diagnostic ultrasonic transducer Regulatory Class: II Product Code: IYN, IYO, and ITX Dated: April 27, 2006 Received: May 2, 2006
Dear Mr. Job:
We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and we have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food. Drug, and Cosmetic Act (Act). You may, therefore, market the device, subject to the general controls provisions of the Act. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration.
This determination of substantial equivalence applies to the following transducers intended for use with the SONOACE PICO Ultrasound System, as described in your premarket notification:
Image /page/2/Picture/11 description: The image shows a circular logo with the letters "FDA" in large, bold font in the center. Above the letters, the years "1906 - 2006" are displayed, indicating a centennial celebration. Below the letters, the word "Centennial" is written in a cursive font, and three stars are aligned beneath it. The text "FDA 100 YEARS OF CONSUMER PROTECTION" is arranged around the circular border of the logo.
{3}------------------------------------------------
Transducer Model Number
| -(1 | AND A . A . A . An . BEACH SECTION1 | LELELE ANNUAL IS LEALERIES & SEA |
|---|---|---|
| 1Andrew | -A bentlette disting10.00------------------------------------------------------------------------------------------------------------------------------------------------------------------------------ | 11And And And Company And And And And And And Children |
| 1 | A 40 1No. of Cattle Catalmore of the comments of the comments of the comments of the comments of the comments of the comments of the comments of the comments of the comments of the comments of the co | .1 |
| AND AND ANDAnd section the different to the desires of the de |
If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to such additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register.
Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.
This determination of substantial equivalence is granted on the condition that prior to shipping the first device. vou submit a postclearance special report. This report should contain complete information, including acoustic output measurements based on production line devices, requested in Appendix G. (enclosed) of the Center's September 30, 1997 "Information for Manufacturers Seeking Marketing Clearance of Diagnostic Ultrasound Systems and Transducers." If the special report is incomplete or contains unacceptable values (e.g., acoustic output greater than approved levels), then the 510(k) clearance may not apply to the production units which as a result may be considered adulterated or misbranded.
The special report should reference the manufacturer's 510(k) number. It should be clearly and prominently marked "ADD-TO-FILE" and should be submitted in duplicate to:
Food and Drug Administration Center for Devices and Radiological Health Document Mail Center (HFZ-401) 9200 Corporate Boulevard Rockville, Maryland 20850
This letter will allow you to begin marketing your device as described in your premarket notification. The FDA finding of substantial equivalence of your device to a legally marketed predicate device results in a classification for your device and thus permits your device to proceed to market.
{4}------------------------------------------------
Page 2 - Mr. Job
If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please contact the Office of Compliance at (240) 276-0120. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). You may obtain other general information on your responsibilities under the Act from the Division of Small Mace Eacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (301) 443-6597 or at its Internet address http://www.fda.gov/cdrh/industry/support/index.html
If you have any questions regarding the content of this letter; please contact Andrew Kang, M.D. at (301) 594-1212.
Sincerely yours,
Nancy C brogdon
Nancy C. Brogdon Director, Division of Reproductive, Abdominal and Radiological Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosures
{5}------------------------------------------------
Section 4.3 INDICATIONS FOR USE
DIAGNOSTIC ULTRASOUND INDICATIONS STATEMENT
061213 510(k) No .:
Device name: SONOACE PICO Ultrasound System Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
Clinical Application Mode of Operation General Specific B M PWD CWD Color Combined* Other (Track I only) (Tracks I & III) Doppler* (Spec.) (Spec.) Ophthalmic Ophthalmic Fetal (Soo Note 3) P P P P Note 1 Nate 7 6 7 8 Abdominal P P P P Note 1 Note 2, 6, 7, 8 Intra-operative (See Note 6) Intra-operative (Neuro.) Fetal Imaging Laparoscopic & Other Pediatric P P P P Note l Note 2, 5, 7, 8 P P P Small Organ (See Note 5) P Note 1 Note 2, 5, 8 N N Neonatal Cephalic N N Note l Note 2, 5, 8 Adult Cephalic P P Trans-rectal P P Note 2, 8 Note 1 Trans-vagina! P P P b Note 2, 3, 8 Note l Trans-urethral Trans-esoph. (non-Cardiac) P P Musculo-skel. (Convent.) P P Notel Note 2, 5, 8 Musculo-skel. (Superfic.) P P P P Note I Note 2, 5, 8 Intra-luminal Other (spec.) P Cardian Adult P P P Notel Note 4 Cardiac Cardiac Pediatric Trans-esophageal (Cardiac) Other (spec.) Perinheral veccal Perinheral P P P P Notel Note 7 5 8 Vessel Other (spec.)
N= new indication; P= previously cleared by FDA in K031552; E= added under Appendix E
Additional Comments:
Color Doppler includes Power (Amplitude) Doppler
Note 1: B/M, B/PWD, B/Color Doppler, B/Power Doppler, B/Color Doppler/PWD, B/Power Doppler/PWD
Note 2: Includes imaging for guidance of biopsy
Note 3: Includes infertility monitoring of follicle development
Note 4: Color M-mode
Note 5: For example: thyroid, parathyroid, breast, scrotum and penis in adult, pediatric and neonatal patients
Note 6: Abdominal organs and peripheral vessel
Note 7: Tissue Harmonic Imaging (THI)
Note 8: 3D Imaging
Concurrence of CDRH, Office of Device Evaluation (ODE) Prescription Use (Per 21 CFR 801.109)
Nancy Brogdon
(Division Sign-Off) D
Division of Reproductive, Abdominal,
and Radiological Devices
510(k) Number K061213
Section 4.3, Page 1 of 12
{6}------------------------------------------------
Kob 1213 510(k) No.: C2-4ES with SONOACE PICO Ultrasound System Device name: Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
| Clinical Application | Mode of Operation | |||||||
|---|---|---|---|---|---|---|---|---|
| General(Track I only) | Specific(Tracks I & III) | B | M | PWD | CWD | ColorDoppler* | Combined*(Spec.) | Other(Spec.) |
| Ophthalmic | Ophthalmic | |||||||
| Fetal (See Note 3) | N | N | N | N | Note 1 | Note 2, 7, 8 | ||
| Abdominal | N | N | N | N | Note 1 | Note 2, 7, 8 | ||
| Intra-operative(Abdominal,vascular) | ||||||||
| Intra-operative (Neuro.) | ||||||||
| Fetal Imaging& Other | Laparoscopic | |||||||
| Pediatric | N | N | N | N | Note 1 | Note 2, 5, 7, 8 | ||
| Small Organ (See Note 5) | ||||||||
| Neonatal Cephalic | ||||||||
| Adult Cephalic | ||||||||
| Trans-rectal | ||||||||
| Trans-vaginal | ||||||||
| Trans-urethral | ||||||||
| Trans-esoph. (non-Cardiac) | ||||||||
| Musculo-skel. (Convent.) | ||||||||
| Musculo-skel. (Superfic.) | ||||||||
| Intra-luminal | ||||||||
| Other (spec.) | ||||||||
| Cardiac | Cardiac Adult | P | P | P | P | Note 1 | Note 4 | |
| Cardiac Pediatric | ||||||||
| Trans-esophageal (Cardiac) | ||||||||
| Other (spec.) | ||||||||
| PeripheralVessel | Peripheral vessel | |||||||
| Other (spec.) |
N= new indication; P= previously cleared by FDA in K031552; E= added under Appendix E
Additional Comments:
Color Doppler includes Power (Amplitude) Doppler
Note 1: B/M, B/PWD, B/Color Doppler, B/Power Doppler, B/Color Doppler/PWD, B/Power Doppler/PWD
Note 2: Includes imaging for guidance of biopsy
Note 3: Includes infertility monitoring of follicle development
Note 4: Color M-mode
Note 5: For example: thyroid, parathyroid, breast, scrotum and penis in adult, pediatric and neonatal patients
Note 6: Abdominal organs and peripheral vessel
Note 7: Tissue Harmonic Imaging (THI)
Note 8: 3D Imaging
Concurrence of CDRH, Office of Device Evaluation (ODE) Prescription Use (Per 21 CFR 801.109)
Nancy broadon
Basic Information
Section 4.3, Page 2 of 12
{7}------------------------------------------------
510(k) No.:
DIAGNOSTIC ULTRASOUND INDICATIONS FOR USE STATEMENT
| Device name: C2-5ET with SONOACE PICO Ultrasound System | ||||||||
|---|---|---|---|---|---|---|---|---|
| Clinical Application | Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:Mode of Operation | |||||||
| General(Track I only) | Specific(Tracks I & III) | B | M | PWD | CWD | ColorDoppler* | Combined*(Spec.) | Other(Spec.) |
| Ophthalmic | Ophthalmic | |||||||
| Fetal (See Note 3) | P | P | P | P | P | Note 1 | Note 2, 7, 8 | |
| Abdominal | P | P | P | P | P | Note 1 | Note 2, 7, 8 | |
| Intra-operative(Abdominal,vascular) | ||||||||
| Intra-operative (Neuro.) | ||||||||
| Fetal Imaging | Laparoscopic | |||||||
| & Other | Pediatric | P | P | P | P | P | Note 1 | Note 2, 7, 8 |
| Small Organ (See Note 5) | ||||||||
| Neonatal Cephalic | ||||||||
| Adult Cephalic | ||||||||
| Trans-rectal | ||||||||
| Trans-vaginal | ||||||||
| Trans-urethral | ||||||||
| Trans-esoph. (non-Cardiac) | ||||||||
| Musculo-skel. (Convent.) | ||||||||
| Musculo-skel. (Superfic.) | ||||||||
| Intra-luminal | ||||||||
| Other (spec.) | ||||||||
| Cardiac Adult | ||||||||
| Cardiac | Cardiac Pediatric | |||||||
| Trans-esophageal (Cardiac) | ||||||||
| Other (spec.) | ||||||||
| Peripheral | Peripheral vessel | |||||||
| Vessel | Other (spec.) |
N= new indication; P= previously cleared by FDA in K043455; E= added under Appendix E Additional Comments:
Color Doppler includes Power (Amplitude) Doppler
Note 1: B/M, B/PWD, B/Color Doppler, B/Power Doppler, B/Color Doppler/PWD, B/Power Doppler/PWD
- Note 2: Includes imaging for guidance of biopsy
Note 3: Includes infertility monitoring of follicle development
Note 4: Color M-mode
Note 5: For example: thyroid, parathyroid, breast, scrotum and penis in adult, pediatric and neonatal patients
- Note 6: Abdominal organs and peripheral vessel
- Note 7: Tissue Harmonic Imaging (THI)
Note 8: 3D Imaging
Concurrence of CDRH, Office of Device Evaluation (ODE) Prescription Use (Per 21 CFR 801.109)
Nancy Brigdon
一、大量的一系的意味
Division of Reproductive, Abdominal,
and Radiological Devices
510(k) Number K061213
Section 4.3, Page 3 of 12
{8}------------------------------------------------
510(k) No .: Device name: th SONOACE PICO Ultrasound System Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
| Clinical Application | Mode of Operation | |||||||
|---|---|---|---|---|---|---|---|---|
| General(Track I only) | Specific(Tracks I & III) | B | M | PWD | CWD | ColorDoppler* | Combined*(Spec.) | Other(Spec.) |
| Ophthalmic | Ophthalmic | |||||||
| Fetal (See Note 3) | P | P | P | P | Note 1 | Note 2, 7, 8 | ||
| Abdominal | P | P | P | P | Note 1 | Note 2, 7, 8 | ||
| Intra-operative (Abdominal, vascular) | ||||||||
| Intra-operative (Neuro.) | ||||||||
| Fetal Imaging& Other | Laparoscopic | |||||||
| Pediatric | P | P | P | P | Note 1 | Note 2, 7, 8 | ||
| Small Organ (See Note 5) | ||||||||
| Neonatal Cephalic | ||||||||
| Adult Cephalic | ||||||||
| Trans-rectal | ||||||||
| Trans-vaginal | ||||||||
| Trans-urethral | ||||||||
| Trans-esoph. (non-Cardiac) | ||||||||
| Musculo-skel. (Convent.) | ||||||||
| Musculo-skel. (Superfic.) | ||||||||
| Intra-luminal | ||||||||
| Other (spec.) | ||||||||
| Cardiac Adult | ||||||||
| Cardiac | Cardiac Pediatric | |||||||
| Trans-esophageal (Cardiac) | ||||||||
| Other (spec.) | ||||||||
| PerinheralVessel | Peripheral vessel | |||||||
| Other (spec.) |
N= new indication; P= previously cleared by FDA in K013627, K031552, K043455; E= added under Appendix E Additional Comments:
Color Doppler includes Power (Amplitude) Doppler
Note 1: B/M, B/PWD, B/Color Doppler, B/Power Doppler, B/Color Doppler/PWD, B/Power Doppler/PWD
Note 2: Includes imaging for guidance of biopsy
Note 3: Includes infertility monitoring of follicle development
Note 4: Color M-mode
Note 5: For example: thyroid, parathyroid, breast, scrotum and penis in adult, pediatric and neonatal patients
Note 6: Abdominal organs and peripheral vessel
Note 7: Tissue Harmonic Imaging (THI)
Note 8: 3D Imaging
Concurrence of CDRH, Office of Device Evaluation (ODE) Prescription Use (Per 21 CFR 801.109)
Nancy C. Brogdon
510kl
Section 4.3, Page 4 of 12
{9}------------------------------------------------
KO61213 510(k) No .:
Device name: C4-7ED with SONOACE PICO Ultrasound System Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
| Clinical Application | Mode of Operation | ||||||||
|---|---|---|---|---|---|---|---|---|---|
| General(Track I only) | Specific(Tracks I & III) | B | M | PWD | CWD | ColorDoppler* | Combined*(Spec.) | Other(Spec.) | |
| Ophthalmic | Ophthalmic | ||||||||
| Fetal (See Note 2) | P | P | P | P | Note 1 | Note 2, 7, 8 | |||
| Abdominal | P | P | P | P | Note 1 | Note 2, 7, 8 | |||
| Intra-operative(Abdominal,vascular) | |||||||||
| Intra-operative (Neuro.) | |||||||||
| Fetal Imaging& Other | Laparoscopic | ||||||||
| Pediatric | P | P | P | P | Note 1 | Note 2, 7, 8 | |||
| Small Organ (See Note 5) | |||||||||
| Neonatal Cephalic | |||||||||
| Adult Cephalic | |||||||||
| Trans-rectal | |||||||||
| Trans-vaginal | |||||||||
| Trans-urethral | |||||||||
| Trans-esoph. (non-Cardiac) | |||||||||
| Musculo-skel. (Convent.) | |||||||||
| Musculo-skel. (Superfic.) | |||||||||
| Intra-luminal | |||||||||
| Other (spec.) | |||||||||
| Cardiac Adult | |||||||||
| Cardiac | Cardiac Pediatric | ||||||||
| Trans-esophageal (Cardiac) | |||||||||
| Other (spec.) | |||||||||
| PerinheralVessel | Perinheral vessel | ||||||||
| Other (spec.) |
N= new indication; P= previously cleared by FDA in K990970, K012887; E= added under Appendix E Additional Comments:
Color Doppler includes Power (Amplitude) Doppler
Note 1: B/M, B/PWD, B/Color Doppler, B/Power Doppler, B/Color Doppler/PWD, B/Power Doppler/PWD
Note 2: Includes imaging for guidance of biopsy
Note 3: Includes infertility monitoring of follicle development
Note 4: Color M-mode
Note 5: For example: thyroid, parathyroid, breast, scrotum and penis in adult, pediatric and neonatal patients
- Note 6: Abdominal organs and peripheral vessel
Note 7: Tissue Harmonic Imaging (THI)
Note 8: 3D Imaging
Concurrence of CDRH, Office of Device Evaluation (ODE) Prescription Use (Per 21 CFR 801.109)
Nancy C. Brogdon
Division of Reproductive, Abdominal,
and Radiological Devices
510(k) Number K061213
Section 4.3, Page 5 of 12
{10}------------------------------------------------
| 510(k) No .: | K061213 | A | ||||||
|---|---|---|---|---|---|---|---|---|
| Device name: | C4-9ED with SONOACE PICO Ultrasound System | |||||||
| Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows: | ||||||||
| Clinical Application | Mode of Operation | |||||||
| General | Specific | B | M | PWD | CWD | Color | Combined* | Other |
| (Track I only) | (Tracks I & III) | Doppler* | (Spec.) | (Spec.) | ||||
| Ophthalmic | Ophthalmic | |||||||
| Fetal (See Note 2) | P | P | P | P | Note 1 | Note 2 6 7 8 | ||
| Abdominal | N | N | N | N | Note 1 | Note 2, 6, 7, 8 | ||
| Intra-operative(Abdominal,vascular) | ||||||||
| Intra-operative (Neuro.) | ||||||||
| Fetal Imaging | Laparoscopic | |||||||
| & Other | Pediatric | N | N | N | N | Note 1 | Note 2, 5, 8 | |
| Small Organ (See Note 5) | P | P | P | P | Note 1 | Note 2, 5, 8 | ||
| Neonatal Cephalic | P | P | P | P | Note 1 | Note 2, 5, 8 | ||
| Adult Cephalic | ||||||||
| Trans-rectal | ||||||||
| Trans-vaginal | ||||||||
| Trans-urethral | ||||||||
| Trans-esoph. (non-Cardiac) | ||||||||
| Musculo-skel. (Convent.) | ||||||||
| Musculo-skel. (Superfic.) | ||||||||
| Intra-luminal | ||||||||
| Other (spec.) | ||||||||
| Cardiac Adult | ||||||||
| Cardiac | Cardiac Pediatric | |||||||
| Trans-esophageal (Cardiac) | ||||||||
| Other (spec.) | ||||||||
| Peripheral | Peripheral vessel | P | P | P | P | Note 1 | Note 2 5 8 | |
| Vessel | Other (spec.) |
N= new indication; P= previously cleared by FDA in K043455; E= added under Appendix E Additional Comments:
Color Doppler includes Power (Amplitude) Doppler
Note 1: B/M, B/PWD, B/Color Doppler, B/Power Doppler, B/Color Doppler/PWD, B/Power Doppler/PWD
- Note 2: Includes imaging for guidance of biopsy
- Note 3: Includes infertility monitoring of follicle development
Note 4: Color M-mode
Note 5: For example: thyroid, parathyroid, breast, scrotum and penis in adult, pediatric and neonatal patients
- Note 6: Abdominal organs and peripheral vessel
- Note 7: Tissue Harmonic Imaging (THI)
Note 8: 3D Imaging
Concurrence of CDRH, Office of Device Evaluation (ODE) Prescription Use (Per 21 CFR 801.109)
Nancy C. Brogdon
(Division Sign Division of Reproductive, Abdo and Radiological Devices 510(k) Number
Section 4.3, Page 6 of 12
.
{11}------------------------------------------------
KO61213 510(k) No .:
Device name: EC4-9ED with SONOACE PICO Ultrasound System Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
Clinical Application Mode of Operation CWD General Specific B M PWD Color Combined* Other (Track I only) (Tracks I & III) Doppler* (Spec.) (Spec.) Ophthalmic Ophthalmic Fetal (Soo Note 3) Abdominal Intra-operative (Abdominal, vascular) Intra-operative (Neuro.) Laparoscopic Fetal Imaging Pediatric & Other Small Organ (See Note 5) Neonatal Cephalic Adult Cephalic Trans-rectal P P P P Note 1 Note 2, 8 P Trans-vaginal P P P Note I Note 2, 3, 8 Trans-urethral Trans-esoph. (non-Cardiac) Musculo-skel. (Convent.) Musculo-skel. (Superfic.) Intra-luminal Other (spec.) Cardian Adult Cardiac Cardiac Pediatric Trans-esophageal (Cardiac) Other (spec.) Perinheral Perinheral vescel Vessel Other (spec.)
N= new indication; P= previously cleared by FDA in K031552, K043455; E=added under Appendix E Additional Comments:
Color Doppler includes Power (Amplitude) Doppler
Note 1: B/M, B/PWD, B/Color Doppler, B/Power Doppler/PWD, B/Power Doppler/PWD, B/Power Doppler/PWD
Note 2: Includes imaging for guidance of biopsy
Note 3: Includes infertility monitoring of follicle development
Note 4: Color M-mode
Note 5: For example: thyroid, breast, scrotum and penis in adult, pediatric and neonatal patients
Note 6: Abdominal organs and peripheral vessel
Note 7: Tissue Harmonic Imaging (THI)
Note 8: 3D Imaging
Concurrence of CDRH, Office of Device Evaluation (ODE) Prescription Use (Per 21 CFR 801.109)
Nancy Brogdon
Basic Information
(Division Sic Division of Reproductiv and Radiological Devices 510(k) Number
Section 4.3, Page 7 of 12
{12}------------------------------------------------
KO61218 510(k) No.:
Device name: EC4-9ES with SONOACE PICO Ultrasound System Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
| Clinical Application | Mode of Operation | ||||||||
|---|---|---|---|---|---|---|---|---|---|
| General(Track I only) | Specific(Tracks I & III) | B | M | PWD | CWD | ColorDoppler* | Combined*(Spec.) | Other(Spec.) | |
| Ophthalmic | Ophthalmic | ||||||||
| Fetal Imaging& Other | Fetal (See Note 3) | ||||||||
| Abdominal | |||||||||
| Intra-operative(Abdominal,vascular) | |||||||||
| Intra-operative (Neuro.) | |||||||||
| Laparoscopic | |||||||||
| Pediatric | |||||||||
| Small Organ (See Note 5) | |||||||||
| Neonatal Cephalic | |||||||||
| Adult Cephalic | |||||||||
| Trans-rectal | P | P | P | P | Note 1 | Note 2, 8 | |||
| Trans-vaginal | P | P | P | P | Note 1 | Note 2, 3, 8 | |||
| Trans-urethral | |||||||||
| Trans-esoph. (non-Cardiac) | |||||||||
| Musculo-skel. (Convent.) | |||||||||
| Musculo-skel. (Superfic.) | |||||||||
| Intra-luminal | |||||||||
| Other (spec.) | |||||||||
| Cardiac | Cardiac Adult | ||||||||
| Cardiac Pediatric | |||||||||
| Trans-esophageal (Cardiac) | |||||||||
| Other (spec.) | |||||||||
| PeripheralVessel | Peripheral vessel | ||||||||
| Other (spec.) |
N=new indication; P= previously cleared by FDA in K031552, K013627; E=added under Appendix E Additional Comments:
Color Doppler includes Power (Amplitude) Doppler
Note 1: B/M, B/PWD, B/Color Doppler, B/Power Doppler, B/Color Doppler/PWD, B/Power Doppler/PWD
Note 2: Includes imaging for guidance of biopsy
Note 3: Includes infertility monitoring of follicle development
Note 4: Color M-mode
Note 5: For example: thyroid, parathyroid, breast, scrotum and penis in adult, pediatric and neonatal patients
Note 6: Abdominal organs and peripheral vessel
Note 7: Tissue Harmonic Imaging (THI)
Note 8: 3D Imaging
Concurrence of CDRH, Office of Device Evaluation (ODE) Prescription Use (Per 21 CFR 801.109)
Nancy C. Brogdon
and Rad 510(k) Numb
Section 4.3, Page 8 of 12
{13}------------------------------------------------
| 510(k) No.: | K061213 | ||||||||
|---|---|---|---|---|---|---|---|---|---|
| Device name: HC2-5ED with SONOACE PICO Ultrasound System | |||||||||
| Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows: | |||||||||
| Clinical Application | Mode of Operation | ||||||||
| General(Track I only) | Specific(Tracks I & III) | B | M | PWD | CWD | ColorDoppler* | Combined*(Spec.) | Other(Spec.) | |
| Ophthalmic | Ophthalmic | ||||||||
| Fetal (See Note 3) | P | P | P | P | Note1 | Note 2 8 | |||
| Abdominal | P | P | P | P | Note1 | Note 2, 8 | |||
| Intra-operative (Abdominal,vascular) | |||||||||
| Intra-operative (Neuro.) | |||||||||
| Fetal Imaging& Other | Laparoscopic | ||||||||
| Pediatric | P | P | P | P | Note1 | Note 2, 8 | |||
| Small Organ (See Note 5) | |||||||||
| Neonatal Cephalic | |||||||||
| Adult Cephalic | |||||||||
| Trans-rectal | |||||||||
| Trans-vaginal | |||||||||
| Trans-urethral | |||||||||
| Trans-esoph. (non-Cardiac) | |||||||||
| Musculo-skel. (Convent.) | |||||||||
| Musculo-skel. (Superfic.) | |||||||||
| Intra-luminal | |||||||||
| Other (spec.) | |||||||||
| Cardiac Adult | |||||||||
| Cardiac | Cardiac Pediatric | ||||||||
| Trans-esophageal (Cardiac) | |||||||||
| Other (spec.) | |||||||||
| PerinheralVessel | Peripheral vesselOther (spec.) |
N= new indication; P= previously cleared by FDA in K031552; E= added under Appendix E Additional Comments:
Color Doppler includes Power (Amplitude) Doppler
Note 1: B/M, B/PWD, B/Color Doppler, B/Power Doppler, B/Color Doppler/PWD, B/Power Doppler/PWD
Note 2: Includes imaging for guidance of biopsy
Note 3: Includes infertility monitoring of follicle development
Note 4: Color M-mode
Note 5: For example: thyroid, parathyroid, breast, scrotum and penis in adult, pediatric and neonatal patients
Note 6: Abdominal organs and peripheral vessel
Note 7: Tissue Harmonic Imaging (THI)
Note 8: 3D Imaging
Concurrence of CDRH, Office of Device Evaluation (ODE) Prescription Use (Per 21 CFR 801.109)
Nancy Broadon
Basic Information
(Division Sio Division of Reproductive and Radiological Devices 510(k) Number
Section 4.3, Page 9 of 12
{14}------------------------------------------------
510(k) No.:
DIAGNOSTIC ULTRASOUND INDICATIONS FOR USE STATEMENT
KO61213
Device name: HL5-9ED with SONOACE PICO Ultrasound System Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
| Clinical ApplicationMode of Operation | ||||||||
|---|---|---|---|---|---|---|---|---|
| General(Track I only) | Specific(Tracks I & III) | B | M | PWD | CWD | ColorDoppler* | Combined*(Spec.) | Other(Spec.) |
| Ophthalmic | Ophthalmic | |||||||
| Fetal ( See Note 3 ) | ||||||||
| Abdominal | ||||||||
| Intra-operative(Abdominal,vascular) | ||||||||
| Intra-operative (Neuro.) | ||||||||
| Fetal Imaging& Other | Laparoscopic | |||||||
| Pediatric | P | P | P | P | Note 1 | Note 2, 5, 8 | ||
| Small Organ ( See Note 5 ) | P | P | P | P | Note 1 | Note 2, 5, 8 | ||
| Neonatal Cephalic | ||||||||
| Adult Cephalic | ||||||||
| Trans-rectal | ||||||||
| Trans-vaginal | ||||||||
| Trans-urethral | ||||||||
| Trans-esoph. (non-Cardiac) | ||||||||
| Musculo-skel. (Convent.) | P | P | P | P | Note 1 | Note 2, 5, 8 | ||
| Musculo-skel. (Superfic.) | P | P | P | P | Note 1 | Note 2, 5, 8 | ||
| Intra-luminal | ||||||||
| Other (spec.) | ||||||||
| Cardiac Adult | ||||||||
| Cardiac | Cardiac Pediatric | |||||||
| Trans-esophageal (Cardiac) | ||||||||
| Other (spec.) | ||||||||
| PerinheralVessel | Perinheral vessel | P | P | P | P | Note 1 | Note 2, 5, 8 | |
| Other (spec.) |
N= new indication; P= previously cleared by FDA in K013627, K031552, K043455; E= added under Appendix E Additional Comments:
Color Doppler includes Power (Amplitude) Doppler
Note 1: B/M, B/PWD, B/Color Doppler, B/Power Doppler, B/Color Doppler/PWD, B/Power Doppler/PWD
- Note 2: Includes imaging for guidance of biopsy
Note 3: Includes infertility monitoring of follicle development
Note 4: Color M-mode
Note 5: For example: thyroid, parathyroid, breast, scrotum and penis in adult, pediatric and neonatal patients
Note 6: Abdominal organs and peripheral vessel
Note 7: Tissue Harmonic Imaging (THI)
Note 8: 3D Imaging
Basic Information
Concurrence of CDRH, Office of Device Evaluation (ODE) Prescription Use (Per 21 CFR 801.109)
Nancy Brogdon
(Division Sign-Division of Reproductive, Abde and Radiological Devices 510(k) Number
Section 4.3, Page 10 of 12
{15}------------------------------------------------
| 510(k) No.: | K061213 | |||||||
|---|---|---|---|---|---|---|---|---|
| Device name: | L5-9EC with SONOACE PICO Ultrasound System | |||||||
| Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows: | ||||||||
| Clinical Application | Mode of Operation | |||||||
| General(Track I only) | Specific(Tracks I & III) | B | M | PWD | CWD | ColorDoppler* | Combined*(Spec.) | Other(Spec.) |
| Ophthalmic | Ophthalmic | |||||||
| Fetal Imaging& Other | Fetal (See Note 3) | |||||||
| Abdominal | ||||||||
| Intra-operative (Abdominal,vascular) | ||||||||
| Intra-operative (Neuro.) | ||||||||
| Laparoscopic | ||||||||
| Pediatric | P | P | P | P | Note 1 | Note 2, 5, 8 | ||
| Small Organ (See Note 5) | P | P | P | P | Note 1 | Note 2, 5, 8 | ||
| Neonatal Cephalic | ||||||||
| Adult Cephalic | ||||||||
| Trans-rectal | ||||||||
| Trans-vaginal | ||||||||
| Trans-urethral | ||||||||
| Trans-esoph. (non-Cardiac) | ||||||||
| Musculo-skel. (Convent.) | P | P | P | P | Note 1 | Note 2, 5, 8 | ||
| Musculo-skel. (Superfic.) | P | P | P | P | Note 1 | Note 2, 5, 8 | ||
| Intra-luminal | ||||||||
| Other (spec.) | ||||||||
| Cardiac | Cardiac Adult | |||||||
| Cardiac Pediatric | ||||||||
| Trans-esophageal (Cardiac) | ||||||||
| Other (spec.) | ||||||||
| PeripheralVessel | Peripheral vessel | P | P | P | P | Note 1 | Note 2 & 8 | |
| Other (spec.) |
| Vessel | Other (spec.) |
|---|---|
| -------- | --------------- |
N= new indication; P= previously cleared by FDA in K013627; E= added under Appendix E
Additional Comments:
Color Doppier includes Power (Amplitude) Doppler
Note 1: B/M, B/PWD, B/Color Doppler, B/Power Doppler, B/Color Doppler/PWD, B/Power Doppler/PWD
Note 2: Includes imaging for guidance of biopsy
Note 3: Includes infertility monitoring of follicle development
Note 4: Color M-mode
Note 5: For example: thyroid, parathyroid, breast, scrotum and penis in adult, pediatric and neonatal patients
Note 6: Abdominal organs and peripheral vessel
Note 7: Tissue Harmonic Imaging (THI)
Note 8: 3D Imaging
Concurrence of CDRH, Office of Device Evaluation (ODE) Prescription Use (Per 21 CFR 801.109)
Nancy C Broadon
(Division Sign-Off) Division of Reproductive, Abdom and Radiological Devices 510(k) Number
Section 4.3, Page 11 of 12
{16}------------------------------------------------
| K061213510(k) No.: | ||||||||
|---|---|---|---|---|---|---|---|---|
| Device name: L5-9EE with SONOACE PICO Ultrasound System | ||||||||
| Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows: | ||||||||
| Clinical Application | Mode of Operation | |||||||
| General(Track I only) | Specific(Tracks I & III) | B | M | PWD | CWD | ColorDoppler* | Combined*(Spec.) | Other(Spec.) |
| Ophthalmic | Ophthalmic | |||||||
| Fetal (See Note 3) | ||||||||
| Abdominal | ||||||||
| Intra-operative(Abdominal,vascular) | ||||||||
| Intra-operative (Neuro.) | ||||||||
| Fetal Imaging& Other | Laparoscopic | |||||||
| Pediatric | P | P | P | P | Note 1 | Note 2, 5, 8 | ||
| Small Organ (See Note 5) | P | P | P | P | Note 1 | Note 2, 5, 8 | ||
| Neonatal Cephalic | ||||||||
| Adult Cephalic | ||||||||
| Trans-rectal | ||||||||
| Trans-vaginal | ||||||||
| Trans-urethral | ||||||||
| Trans-esoph. (non-Cardiac) | ||||||||
| Musculo-skel. (Convent.) | P | P | P | P | Note 1 | Note 2, 5, 8 | ||
| Musculo-skel. (Superfic.) | P | P | P | P | Note 1 | Note 2, 5, 8 | ||
| Intra-luminal | ||||||||
| Other (spec.) | ||||||||
| Cardiac Adult | ||||||||
| Cardiac | Cardiac Pediatric | |||||||
| Trans-esophageal (Cardiac) | ||||||||
| Other (spec.) | ||||||||
| PeripheralVessel | Peripheral vessel | P | P | P | P | Note 1 | Note 2, 8 | |
| Other (spec.) |
N= new indication; P= previously cleared by FDA in K043455; E= added under Appendix E
Additional Comments:
Color Doppler includes Power (Amplitude) Doppler
Note 1: B/M, B/PWD, B/Color Doppler, B/Power Doppler, B/Color Doppler/PWD, B/Power Doppler/PWD
Note 2: Includes imaging for guidance of biopsy
Note 3: Includes infertility monitoring of follicle development
Note 4: Color M-mode
Note 5: For example: thyroid, parathyroid, breast, scrotum and penis in adult, pediatric and neonatal patients
Note 6: Abdominal organs and peripheral vessel
Note 7: Tissue Harmonic Imaging (THI)
Note 8: 3D Imaging
Concurrence of CDRH, Office of Device Evaluation (ODE) Prescription Use (Per 21 CFR 801.109)
Nancy Chogdon
Basic Information
(Division Sign Division of Reproductive, A and Radiological Devices " : " : " : imhor
Section 4.3, Page 12 of 12
§ 892.1550 Ultrasonic pulsed doppler imaging system.
(a)
Identification. An ultrasonic pulsed doppler imaging system is a device that combines the features of continuous wave doppler-effect technology with pulsed-echo effect technology and is intended to determine stationary body tissue characteristics, such as depth or location of tissue interfaces or dynamic tissue characteristics such as velocity of blood or tissue motion. This generic type of device may include signal analysis and display equipment, patient and equipment supports, component parts, and accessories.(b)
Classification. Class II.