(30 days)
Not Found
No
The document explicitly states that "All parameters within the hard-coding of the VascuView TAP software program are fixed," indicating a lack of adaptive or learning capabilities characteristic of AI/ML. There is no mention of AI, ML, or related concepts like neural networks or training data.
No
Explanation: The device is described as an "ultrasonic imaging system intended for diagnostic imaging" and "real-time viewing of peripheral vascular structures...to provide guidance for the placement of needles and catheters." It is not described as providing treatment.
Yes
Explanation: The "Intended Use / Indications for Use" section explicitly states that the device "is intended for diagnostic imaging of the human body." Additionally, the "Device Description" mentions its use for "assisted vascular access of veins and arteries, in addition to other vascular access applications such as the real-time viewing of peripheral vascular structures and their surrounding regions in order to provide guidance for the placement of needles and catheters within these structures," which is a diagnostic application. The "Predicate Device(s)" also list diagnostic ultrasound systems.
No
The device description explicitly lists hardware components including a Tablet PC, an Ultrasound Beam-former PCB, and a 64-element Linear Array Probe, in addition to the software.
Based on the provided text, the VascuView TAP Ultrasound System is not an In Vitro Diagnostic (IVD) device.
Here's why:
- Definition of IVD: In Vitro Diagnostics are medical devices used to perform tests on samples taken from the human body, such as blood, urine, or tissue, to provide information about a person's health. These tests are performed outside of the living body (in vitro).
- VascuView TAP Function: The description clearly states that the VascuView TAP Ultrasound System is intended for "diagnostic imaging of the human body" and "transmits ultrasonic energy into patients, then perform post-processing of received echoes to generate on-screen display of anatomic structures within the body." This is a form of in vivo (within the living body) diagnostic imaging.
- No Mention of Samples: The text does not mention the collection or analysis of any biological samples from the patient.
Therefore, the VascuView TAP Ultrasound System falls under the category of medical imaging devices used for in vivo diagnosis, not In Vitro Diagnostics.
N/A
Intended Use / Indications for Use
The VascuView TAP Ultrasound System with probe Model #HL.7.5/40/64D is intended for diagnostic imaging of the human body for the following clinical applications, as illustrated in the Diagnostic Indications for Use Form which can be found in Attachment 5A: Pediatric, Musculo-skeletal (Conventional), Musculo-skeletal (Superficial), Peripheral Vessels which include Intra-Venous and Perioherally-Inserted Central Catheters, as well as vascular structures and surrounding vascular regions such as nerve bundles and various structures for free hand placement of needles and catheters. The VascuView TAP Ultrasound System is not intended for fetal or ophthalmic applications.
The VascuView TAP ultrasound system provides ultrasound imaging of peripheral vascular structures in order to provide for ultrasound guidance for placement of needles and catheters in these structures. The VascuView TAP is also used for ultrasound imaging of vascular structures and surrounding regions of the vascular such as nerve bundles and various structures.
The VascuView TAP ultrasound system is not intended for fetal or ophthalmic applications.
Product codes (comma separated list FDA assigned to the subject device)
90-IYO, 90-ITX, 90-IYN
Device Description
The VascuView TAP Ultrasound System is a high-frequency ultrasonic imaging system intended to be used for assisted vascular access of veins and arteries, in addition to other vascular access applications such as the real-time viewing of perigheral vascular structures and their surrounding regions in order to provide quidance for the placement of needles and catheters within these structures. The system software runs on Windows XP Professional Operating System and utilizes features of the Windows interface to direct the operation of the system and maintain patient records; providing a user-friendly environment for clinical applications. The VascuView TAP System consists of the following components:
- UL and TUV 60950 Approved Tablet PC with Integrated Outer Enclosure . A Kiosk tablet oc is provided with a UL approved Medical-grade power supply and Medical-grade power cord. The VascuView TAP ultrasound system consists of an integrated carrying handle. probe holder, cord wrap, table stand, and shock absorbent corner bumpers. The pc includes a large 12.1" TFT XGA LCD wide angle display which facilitates an intuitive touch screen control interface with clear-cut functionality and preset settings to ameliorate image optimization. Additionally, the oc provides for the operation of the software, as well as the storage of archived images and video clips.
- . Ultrasound Beam-former PCB with 64-element Linear Array Probe The handheld ultrasound probe Model #HL7.5/40/64D and beam-former PCB consists of a sixtyfour element pulsed linear array capable of capturing both images and videos in four different modes of operation: B-Mode, Split Screen Dual B-Mode, Color Doppler (CFM), and B-Mode with Doppler (PWD). The probe is connected to the pc via the included SCSI cable and operates within a frequency range of 5MHz -- 10MHz, which allows for the visualization of surface vessels at scan depths up to 9cm. The transducer material is made of a gold plated polymer membrane and a biocompatible nose cone sufficient for its use (Silicon).
- . VascuView TAP System Software
All features and controls of the system are provided for in the VascuView TAP software which comes pre-loaded onto the tablet pc. The software uses an icon-based interface whereby the user can select any of the primary functional screens at any time by clicking on an icon located on the screen, for that function. The software enables ultrasound image storage and display, measurement functions, enhancements, and printing. All parameters within the hard-coding of the VascuView TAP software program are fixed, therefore the user cannot make any adjustments to the operation of the transducer that will have an effect on the radiated field (i.e. center frequency, aperture, focus, field of view, sample rate, etc.)
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Ultrasound
Anatomical Site
Human body, Pediatric, Musculo-skeletal (Conventional), Musculo-skeletal (Superficial), Peripheral Vessels (Intra-Venous and Peripherally-Inserted Central Catheters), vascular structures, nerve bundles, various structures.
Indicated Patient Age Range
Not Found
Intended User / Care Setting
Not Found
Description of the training set, sample size, data source, and annotation protocol
Not Found
Description of the test set, sample size, data source, and annotation protocol
Not Found
Summary of Performance Studies (study type, sample size, AUC, MRMC, standalone performance, key results)
Non-Clinical Performance Data: The VascuView TAP was assessed as compliant with international safety standards, including IEC 60601-1, IEC 60601-1-2, IEC 60601-1-4, and IEC 60601-2-37 (including acoustic output limits). Measurement accuracy was confirmed via a measurement validation test protocol (Attachment 8A Measurement Accuracy Validation Report) using an ATS model 539 phantom with 0.7 dB/cm-MHz attenuation. The software has also been validated using a test protocol.
Clinical Performance Data: None submitted.
Conclusions: Based on the non-clinical data, the VascuView TAP system has demonstrated that it is as safe, as effective, performs as well as or better than the predicate devices, and includes similar design characteristics and intended use.
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
Not Found
Predicate Device(s): If the device was cleared using the 510(k) pathway, identify the Predicate Device(s) K/DEN number used to claim substantial equivalence and list them here in a comma separated list exactly as they appear in the text. List the primary predicate first in the list.
Reference Device(s): Identify the Reference Device(s) K/DEN number and list them here in a comma separated list exactly as they appear in the text.
Not Found
Predetermined Change Control Plan (PCCP) - All Relevant Information for the subject device only (e.g. presence / absence, what scope was granted / cleared under the PCCP, any restrictions, etc).
Not Found
§ 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.
0
K09 3da3
2440 South 179th Street New Berlin, WI 53146 Tel 800-433-8197 Fax 262-821-9927 www.escalonvascularaccess.com
Image /page/0/Picture/3 description: The image is a logo for Escalon Vascular Access, a division of Escalon Medical Corp. The logo features a stylized "VA" with a catheter running through it horizontally. To the right of the "VA" is a symbol resembling radio waves or a signal, possibly representing access or communication.
Summary of Safety and Effectiveness Information
This summary of 510(k) safety and effectiveness for the VascuView TAP™ Ultrasound System is being submitted in accordance with the requirements of the Safe Medical Devices Act (SMDA) of 1990 and the Premarket Notification Procedures of 21 CFR; Part 807, Subpart E, Section 807.92 upon which the substantial equivalence (SE) determination is based.
| Submitter's Name | Escalon Medical Corp
2440 South 179th Street
New Berlin, WI 53146
800-433-8197 262-821-9182
Fax 262-821-9927 |
|------------------------|----------------------------------------------------------------------------------------------------------------------------|
| Contact Person | Roger Edens
Vice-President Engineering
Tel: (262) 821-9182
Fax: (262) 821-9927
reddens@escalonmed.com |
| Date of Preparation | October 13, 2009 |
| Device Trade Name | VascuView TAP™ Ultrasound System |
| Common Name(s) | Ultrasonic Pulsed Echo Imaging System
Diagnostic Ultrasound Transducer |
| Classification Name(s) | Ultrasonic Pulsed Echo Imaging System
FR Number: 892.1560
Product Code: 90-IYO |
| | Diagnostic Ultrasound Transducer
FR Number: 892-1570
Product Code: 90-ITX |
| | Ultrasonic Pulsed Doppler Imaging System
FR Number: 892-1550
Product Code: 90-IYN |
| Device Classification | Class II |
| Predicate Device(s) | SONOACE PICO Diagnostic Ultrasound System
510(k) Number: K061213
SE Clearance Date: May 16, 2006 |
| | Sonosite iLook 25 Personal Imaging Tool
510(k) Number: K033367
SE Clearance Date: November 5, 2003 |
DEC 2 3 2009
1
VascuView TAP Device Description
The VascuView TAP Ultrasound System is a high-frequency ultrasonic imaging system intended to be used for assisted vascular access of veins and arteries, in addition to other vascular access applications such as the real-time viewing of perigheral vascular structures and their surrounding regions in order to provide quidance for the placement of needles and catheters within these structures. The system software runs on Windows XP Professional Operating System and utilizes features of the Windows interface to direct the operation of the system and maintain patient records; providing a user-friendly environment for clinical applications. The VascuView TAP System consists of the following components:
- UL and TUV 60950 Approved Tablet PC with Integrated Outer Enclosure . A Kiosk tablet oc is provided with a UL approved Medical-grade power supply and Medical-grade power cord. The VascuView TAP ultrasound system consists of an integrated carrying handle. probe holder, cord wrap, table stand, and shock absorbent corner bumpers. The pc includes a large 12.1" TFT XGA LCD wide angle display which facilitates an intuitive touch screen control interface with clear-cut functionality and preset settings to ameliorate image optimization. Additionally, the oc provides for the operation of the software, as well as the storage of archived images and video clips.
- . Ultrasound Beam-former PCB with 64-element Linear Array Probe The handheld ultrasound probe Model #HL7.5/40/64D and beam-former PCB consists of a sixtyfour element pulsed linear array capable of capturing both images and videos in four different modes of operation: B-Mode, Split Screen Dual B-Mode, Color Doppler (CFM), and B-Mode with Doppler (PWD). The probe is connected to the pc via the included SCSI cable and operates within a frequency range of 5MHz -- 10MHz, which allows for the visualization of surface vessels at scan depths up to 9cm. The transducer material is made of a gold plated polymer membrane and a biocompatible nose cone sufficient for its use (Silicon).
- . VascuView TAP System Software
All features and controls of the system are provided for in the VascuView TAP software which comes pre-loaded onto the tablet pc. The software uses an icon-based interface whereby the user can select any of the primary functional screens at any time by clicking on an icon located on the screen, for that function. The software enables ultrasound image storage and display, measurement functions, enhancements, and printing. All parameters within the hard-coding of the VascuView TAP software program are fixed, therefore the user cannot make any adjustments to the operation of the transducer that will have an effect on the radiated field (i.e. center frequency, aperture, focus, field of view, sample rate, etc.)
The VascuView TAP Ultrasound System has been designed, as applicable to its features, to comply with the following product safety standards listed in the table below.
| IEC
Standard | IEC 60601-1:2005 Medical Electrical Equipment: Part 1 - General Requirements for Safety IEC 60601-1-1:2000 Medical Electrical Equipment Collateral Standard: Safety Requirements for Medical
Electrical Systems IEC 60601-1-2:2001 Medical Electrical Equipment Collateral Standard: Electromagnetic Compatibility IEC 60601-1-4:1996 Medical Electrical Equipment Collateral Standard: Part 4: Safety Requirements for
Programmable Electronic Medical Systems IEC 60601-2-37:2004 Medical Electrical Equipment: Part 2 - Particular Requirements for the Safety of
Ultrasonic Medical Diagnostic and Monitoring |
|-------------------|----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| EN
Standard | EN 61000-3-2:2000 Limits for Harmonic Current Emissions EN 61000-3-3:1995 Electromagnetic Compatibility: Limitation of Voltage Fluctuation and Flicker in Low-
Voltage Supply Systems with Rated Current Up to 16 Amps EN 55011: 1998 (A1:1999) Group 1, Class A for Industrial, Scientific, and Medical (ISM) Equipment |
| CISPR
Standard | CISPR 11:2004 Group 1, Class A, for Industrial, Scientific, and Medical (ISM) Equipment: Radio
Frequency Equipment Electromagnetic Disturbance Characteristics Limits and Methods of Measurement |
| ISO
Standard | ISO 14971:2007 Medical Devices - Applications of Risk Management to Medical Devices ISO 13485:2003 Medical Devices Quality Management Systems - Requirements for Regulatory Purposes ISO 10993-1:2009 Biological Evaluation of Medical Devices Part 1 -- Evaluation and Testing within a Risk
Management Process ISO 10993-5:2009 Biological Evaluation of Medical Devices: Part 5 - Tests for In Vitro Cytoxicity ISO 10993-10:2002 Biological Evaluation of Medical Devices: Part 10 - Tests for Irritation and Delayed-
Type Hypersensitivity ISO 10993-11:2006 Biological Evaluation of Medical Devices: Part 11 - Tests for Systemic Toxicity |
2
Intended Use / Indications for Use
The VascuView TAP Ultrasound System with probe Model #HL.7.5/40/64D is intended for diagnostic imaging of the human body for the following clinical applications, as illustrated in the Diagnostic Indications for Use Form which can be found in Attachment 5A: Pediatric, Musculo-skeletal (Conventional), Musculo-skeletal (Superficial), Peripheral Vessels which include Intra-Venous and Perioherally-Inserted Central Catheters, as well as vascular structures and surrounding vascular regions such as nerve bundles and various structures for free hand placement of needles/catheters. The VascuView TAP Ultrasound System is not intended for fetal or ophthalmic applications.
Device Technology Characteristics and Comparison to Predicate Device(s)
The legally marketed predicate device(s) to which the VascuView TAP Ultrasound System is considered substantially equivalent through the 510(k) premarket notification process are the SONOACE PICO Diagnostic Ultrasound System cleared under K061213 and the SonoSite® iLook 25 Ultrasound System cleared under K033367.
Based on the Comparison with Predicate Devices as shown in the table illustrated in Section 6 of this 510(k) submission, as per the guidance of FDA Substantial Equivalence recommendations, the VascuView TAP Ultrasound System is deemed sufficient in the demonstration of substantial equivalence to both predicate devices. A summarization of the similarities and differences between the VascuView TAP and each of the proposed predicate devices is discussed below.
| Proprietary Device Name | SONOACE PICO Diagnostic Ultrasound System | SonoSite® iLook 25 Ultrasound System |
|---|---|---|
| Trade Name | SONOACE PICO Ultrasound System | iLook 25 Ultrasound System |
| 510(k) Submitter/Holder | Medison, Co., Ltd. | SonoSite, Inc. |
| 510(k) Number | K061213 | K03367 |
| Regulatory Class | Class II | Class II |
| Regulation Number | 21 CFR 892.1550 | 21 CFR 892.1550 |
| Classification Product Code | IYN | IYN |
Summary for explanation of the Predicate Device(s) Technological Characteristics
Similarities of the SONOACE PICO and the VascuView TAP include:
- . Both systems are intended for Pediatric, Vascular, and Musculoskeletal applications.
- Both systems are mobile, software-controlled systems whose function is to acquire ultrasound . data and to display the data in different imaging modes.
- Both systems are capable of displaying images in the following modes of operation: 2D B-Mode, . Color Doppler (CFM), and B-Mode with Doppler (PWD).
- Both systems possess linear measurement capabilities. .
- Both systems include a 64-element linear array probe design operating within a frequency range . of 5MHz - 10MHz.
- Both systems have an LCD display .
- . Both systems include Cine review capabilities.
- Both systems transmit ultrasonic energy into patients. then perform post-processing of received . echoes to generate on-screen display of anatomic structures within the body.
- . Both systems allow for specialized measurements of structures.
- . Both systems provide for on-screen display of thermal and mechanical indices related to potential bio-effect mechanisms
Differences of the SONOACE PICO and the VascuView TAP include:
- . The SONOACE PICO is a dedicated device, while the VascuView TAP system utilizes a tablet pc set up to launch immediately into the VascuView TAP software.
- The VascuView TAP provides for a larger screen to aid in visualization. .
- The SQNOACE PICO offers M-Mode Imaging, Tissue Harmonic Imaging, Trapezoidal Imaging, . and freehand 3D imaging tools of which are not provided for in the Vascuview TAP.
- The SONOACE PICO indications for use includes: fetal applications, whereas the VascuView . TAP is not.
3
Similarities of the SonoSite® iLook 25 Ultrasound System and the VascuView TAP include:
- Both systems are intended for Pediatric, Vascular, and Musculoskeletal (both conventional and . superficial), and Peripheral Vessel applications.
- . Both systems are highly portable, software-controlled systems whose function is to acquire ultrasound data and to display the data in different imaging modes.
- Both systems are capable of displaying images in the following modes of operation: 2D B-Mode, . and Color Doppier (CFM) Mode.
- . Both systems possess linear measurement capabilities which incorporate a linear array probe and beamformer (pulser and receiver) circuitry.
- . Both systems provide controls for touch screen data input, menu, freeze, patient information, save and power.
- . Both systems provide a power Doppler mode that displays different colors (red or blue) by determining directionality of blood flow within vessels which, given the anatomical location of the vessel and orientation of the ultrasound probe.
- . Both systems assist the user in determining whether a vessel is a vein or artery by allowing for the observation of whether the vessel is pulsing (indicating an artery) or not (indicating a vein), in addition to anatomical location.
- Both systems include Cine review to retain images for frame-by-frame viewing. .
- Both systems provide for system optimization presets and a crystal display with brightness and . contrast controls.
Differences of the SonoSite® iLook 25 Ultrasound System and the VascuView TAP include:
- The SonoSite® iLook 25 is a dedicated device, while the VascuView TAP system utilizes a tablet . pc set up to launch immediately into the VascuView TAP software.
- . The VascuView TAP provides for a larger screen to aid in visualization; approximately 4x greater in viewing area.
- . The SonoSite® iLook 25 is limited to an internal storage capacity of 74 images, while the VascuView TAP system has virtually unlimited storage (tens of thousands of images on tablet pc hard drive and ability to connect external hard drives if additional storage is required).
- The SonoSite® iLook 25 indications for use includes: fetal applications, whereas the VascuView . TAP is not.
Non-Clinical Performance Data
The VascuView TAP will be assessed as verified as compliant with the requirements of several international safety standards, including IEC 60601-1, IEC 60601-1-2, IEC 60601-1-4, and IEC 60601-2-37 (including acoustic output limits), and others. Additionally, the measurement accuracy of the VascuView TAP system was confirmed via a measurement validation test protocol (Attachment 8A Measurement Accuracy Validation Report) using an ATS model 539 phantom with 0.7 dB/cm-MHz attenuation. The software has been also been validated using a test protocol.
Clinical Performance Data
None submitted.
Conclusions from Non-Clinical (and Clinical) Data
Based upon the results of the data as summarized above, the VascuView TAP system has demonstrated that it is as safe, as effective, performs as well as or better than the predicate devices, and includes similar design characteristics and intended use. Furthermore, based on the comparison with the predicate devices as shown in the discussion above, as well as guidance provided by FDA 510(k) Substantial Equivalence Decision-Making Process Flowchart, the Escalon Vascular Access VascuView TAP ultrasound system is deemed to be substantially equivalent to the proposed predicate devices.
4
Image /page/4/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo features a stylized eagle-like symbol with three lines forming its body and wings. The text "DEPARTMENT OF HEALTH & HUMAN SERVICES • USA" is arranged in a circular fashion around the symbol.
DEC 2 3 2009
Food and Drug Administration 10903 New Hampshire Avenue Document Mail Center - WO66-G609 Silver Spring, MD 20993-0002
: '
Escalon Medical Corporation % Mr. Mark Job Responsible Third Party Official Regulatory Technology Services LLC 1394 25th Street NW BUFFALO MN 55313
Re: K093613
Trade/Device Name: VU65000 - VascuView TAP Ultrasound System Regulation Number: 21 CFR 892.1550 Regulation Name: Ultrasonic pulsed doppler imaging system Regulatory Class: II Product Code: IYN, IYO, and ITX Dated: December 16, 2009 Received: December 17, 2009
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 VU65000 - VascuView TAP Ultrasound System, as described in your premarket notification:
Transducer Model Number
HL7.5/40/64D
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.
5
Page 2 - Mr. Job
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 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.
If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please go to http://www.fda.gov/AboutFDA/CentersOffices/CDRH/CDRHOffices/ucm115809.htm for the Center for Devices and Radiological Health's (CDRH's) Office of Compliance. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to
http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm for the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance.
If you have any questions regarding the content of this letter, please contact Shahram Vaezy at (301) 796-6242.
Sincerely vours.
Joha C. Myri
for
Janine M. Morris Acting Director, Division of Reproductive, Abdominal, and Radiological Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure(s)
6
Indications for Use
510(k) Number (if known):
K0936/3
Device Name:
Indications For Use:
VascuView TAP Ultrasound System
The VascuView TAP ultrasound system provides ultrasound imaging of peripheral vascular structures in order to provide for ultrasound guidance for placement of needles and catheters in these structures. The VascuView TAP is also used for ultrasound imaging of vascular structures and surrounding regions of the vascular such as nerve bundles and various structures.
The VascuView TAP ultrasound system is not intended for fetal or ophthalmic applications.
× Prescription Use (Part 21 CFR 801 Subpart D) AND/OR
Over-The-Counter Use (21. CFR 801 Subpart C)
(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)
Concurrence of CDRH, Office of Device Evaluation (ODE)
_
(Division Sign-Off)_
Division of Reproductive, Abdominal. and Radiological Devices 510(k) Number.
Page 1 of
7
Appendix G
Appendix G: Diagnostic Ultrasound Indications For Use Form
VU65000 - Vascu/iew TAP Ultrasound System System:
Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
| Clinical Application | Modes of Operations | |||||||
|---|---|---|---|---|---|---|---|---|
| Specific | ||||||||
| (Tracks 1 & 3) | B | M | PWD | CWD | Color | |||
| Doppler | Combined | |||||||
| (Specify) | Other* | |||||||
| (Specify) | ||||||||
| General | ||||||||
| (Track 1 Only) | Opthalmic | |||||||
| Opthalmic | Fetal | |||||||
| Abdominal | ||||||||
| Intra-operative (Specify) | ||||||||
| Intra-operative (Neuro) | ||||||||
| Laparoscopic | ||||||||
| Pediatric | N | N | N | Note [1] | ||||
| Small Organ (Specify) | ||||||||
| Neonatal Cephalic | ||||||||
| Fetal | ||||||||
| Imaging | ||||||||
| & Other | Adult Cephalic | |||||||
| Trans-rectal | ||||||||
| Trans-vaginal | ||||||||
| Trans-urethral | ||||||||
| Trans-esoph. (non-Card.) | ||||||||
| Musculo-skeletal | ||||||||
| (Conventional) | N | N | N | Note [1] | ||||
| Musculo-skeletal | ||||||||
| (Superficial) | N | N | N | Note [1] | ||||
| Intravascular | ||||||||
| Other (Specify) | ||||||||
| Cardiac | Cardiac Adult | |||||||
| Cardiac Pediatric | ||||||||
| Intravascular (Cardiac) | ||||||||
| Trans-esoph. (Cardiac) | ||||||||
| Intra-cardiac | ||||||||
| Other (Specify) | ||||||||
| Peripheral | ||||||||
| Vessel | Peripheral Vessel Note [2] | N | N | N | Note [1] | |||
| Other (Specify) Note [3] | N | N | N | Note [1] |
N = new indication; P = previously cleared by FDA; E = added under this appendix
*Example of other modes of operation may include: A-mode, Amplitude Doppler, 3-D Imaging, Harmonic Imaging, Tissue Motion Doppler, and Color Velocity Imaging for prescription use.
Notes:
- [1] B+PW, B+Color Doppler
- [2] Includes Intra-Venous, Peripherally-Inserted Central Catheters
- [3] Imaging of vascular structures and surrounding regions of the yascular such as nerve bundles and various structures for free hand placement of needles/catheters.
Nommhing
(Division Sign-Off) Division of Reproductive, Abdominal and Radiological Device
510(k) Number K0436
8
Appendix G
Appendix G: Diagnostic Ultrasound Indications For Use Form
VU65000 - VascuView TAP Ultrasound System System: Probe Model #HL7 5/40/64D Transducer:
Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
| Clinical Application | Modes of Operations | |||||||
|---|---|---|---|---|---|---|---|---|
| General | ||||||||
| (Track 1 Only) | Specific | |||||||
| (Tracks 1 & 3) | B | M | PWD | CWD | Color Doppler | Combined (Specify) | Other* (Specify) | |
| Opthalmic | Opthalmic | |||||||
| Fetal | ||||||||
| Abdominal | ||||||||
| Intra-operative (Specify) | ||||||||
| Intra-operative (Neuro) | ||||||||
| Laparoscopic | ||||||||
| Pediatric | N | N | N | N | Note [1] | |||
| Small Organ (Specify) | ||||||||
| Neonatal Cephalic | ||||||||
| Fetal | ||||||||
| Imaging | ||||||||
| & Other | Adult Cephalic | |||||||
| Trans-rectal | ||||||||
| Trans-vaginal | ||||||||
| Trans-urethral | ||||||||
| Trans-esoph. (non-Card.) | ||||||||
| Musculo-skeletal | ||||||||
| (Conventional) | N | N | N | N | Note [1] | |||
| Musculo-skeletal | ||||||||
| (Superficial) | N | N | N | N | Note [1] | |||
| Intravascular | ||||||||
| Other (Specify) | ||||||||
| Cardiac Adult | ||||||||
| Cardiac | Cardiac Pediatric | |||||||
| Intravascular (Cardiac) | ||||||||
| Trans-esoph. (Cardiac) | ||||||||
| Intra-cardiac | ||||||||
| Other (Specify) | ||||||||
| Peripheral | ||||||||
| Vessel | Peripheral Vessel Note [2] | N | N | N | N | Note [1] | ||
| Other (Specify) Note [3] | N | N | N | N | Note [1] |
N = new indication; P = previously cleared by FDA; E = added under this appendix
*Example of other modes of operation may include: A-mode, Amplitude Doppler, 3-D Imaging, Harmonic Imaging, Tissue Motion Doppler, and Color Velocity Imaging for prescription use.
Notes:
- [1] B+PW. B+Color Doppler
- [2] Includes Intra-Venous, Peripherally-Inserted Central Catheters
- [3] Imaging of vascular structures and surrounding regions of the vascular such as nerve bundles and various structures for free hand placement of needles/catheters.
Norm Whing
(Division Sign-Off)
Division of Reproductive, Abdominal. and Radiological Devi
510(k) Number K0936