(22 days)
Not Found
No
The summary describes a standard ultrasound device that calculates volume based on multiple scan planes. There is no mention of AI, ML, or any advanced image processing techniques that would suggest the use of such technologies. The volume calculation appears to be based on geometric principles applied to the acquired images.
No
The device is used to measure urine volume and obtain images for diagnostic purposes, not to treat a condition or restore a function.
Yes
The device "obtains images of the bladder to calculate the urine volume non-invasively" and "non-invasively measures the urine in the bladder". While it calculates a volume, this calculation is based on obtaining images of an internal organ to gain information about a patient's physiological state (e.g., urine retention), which functions as a form of diagnosis.
No
The device description explicitly states it is a "B-mode instrument, hand-held, wireless and battery-operated" with a "3D-mechnical sector transducer," indicating it includes significant hardware components beyond just software.
Based on the provided information, the BioCon-900 is not an In Vitro Diagnostic (IVD) device.
Here's why:
- IVD Definition: In Vitro Diagnostic devices are used to examine specimens (like blood, urine, or tissue) taken from the human body to provide information about a person's health.
- BioCon-900 Function: The BioCon-900 uses ultrasound to non-invasively measure the volume of urine within the bladder. It does not analyze a specimen taken from the body.
The BioCon-900 is a medical device that uses imaging (ultrasound) to assess a physiological state (bladder volume) directly within the patient's body. This falls under the category of imaging or diagnostic devices, but not IVD.
N/A
Intended Use / Indications for Use
BioCon-900 is a B-mode pulsed-echo ultrasound device. The BioCon-900 projects ultrasonic energy through the lower of a patient to obtain images of the bladder to calculate the urine volume non-invasively. BioCon-900 is intended to be used by a qualified medical professional to non-invasively measure the urine in the bladder. Contraindications for the BioCon-900 are fetal use and use on pregnant patients.
BioCon-900 projects ultrasonic energy through the lower abdomen of a patient to obtain images of bladder to calculate the urine volume non-invasively.
Product codes (comma separated list FDA assigned to the subject device)
IYO, ITX
Device Description
CUBEScan™ BioCon-900 (bladder volume measurement system) is a safe and easy, non-invasive system to measure the bladder volume. CUBEScan™ BioCon-900 is a B-mode instrument, hand-held, wireless and battery-operated. A 3D-mechnical sector transducer provides cross-sectional images of the bladder from up to 12 scan planes and bladder volume is calculated based upon those images and displays 12 scan planes on a screen. Furthermore, a live image of the bladder during Pre-Scan makes it easier to detect the bladder before scanning. Measurements are transmitted to a personal computer running CubePro software via a wireless connection. CubePro allows the user to print measurements, archive data and so on.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
B-mode pulsed-echo ultrasound
Anatomical Site
lower abdomen / bladder
Indicated Patient Age Range
Not Found
Intended User / Care Setting
qualified medical professional
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)
Biocompatibility Testing: The biocompatibility test for CUBEScan™ BioCon-900 was conducted in accordance with ISO-10993 as recognized by FDA. The following tests performed: Cytotoxicity Test (MEM Elution Test), Maximization Sensation, Intracutaneous Reactivity.
Electrical Safety and Electromagnetic Compatibility (EMC): Electrical safety and EMC testing were conducted on the CUBEScan™ BioCon-900. The CUBEScan™ BioCon-900 complied with AAMI/ANSI ES 6060-1, IEC6060-1-2 for safety and EMC including battery, Ir communication, barcode and wireless charging.
Acoustic Output Testing: The acoustic output test for was CUBEScant™ BioCon-900 conducted in accordance with IEC60601-2-37.
Software Validation: Software Validation testing for CUBEScan™ BioCon-900 was conducted and documentation was provided as recommended "Guidance for the Content of Premarket Submissions for Software in Medical Devices".
Volume Measuring Testing: In order to demonstrate the accuracy of CUBEScan™ BioCon-900, a tissue-equivalent bladder phantom with a balloon which has a designated volume is used. The accuracy has been demonstrated by designated volume to the volume from CUBEScan™ BioCon-900.
Wireless Telecommunication & Charging: The CUBEScan 114 BioCon-900 is intended for use in an environment in which radiated RF disturbances are controlled. In order to demonstrate the safety of RF communications, Wireless Telecommunication Testing was conducted in accordance with 47 CFR FCC - Telecommunications, Chapter I - Federal Communications Commission, Subchapter A - General Part 15 - Radiofrequency Devices Subpart C section 15.207/15.209 and RF Exposure.
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
§ 892.1560 Ultrasonic pulsed echo imaging system.
(a)
Identification. An ultrasonic pulsed echo imaging system is a device intended to project a pulsed sound beam into body tissue to determine the depth or location of the tissue interfaces and to measure the duration of an acoustic pulse from the transmitter to the tissue interface and back to the receiver. This generic type of device may include signal analysis and display equipment, patient and equipment supports, component parts, and accessories.(b)
Classification. Class II (special controls). A biopsy needle guide kit intended for use with an ultrasonic pulsed echo imaging system only is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 892.9.
0
Image /page/0/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo is a circular seal with the words "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" around the perimeter. Inside the circle is a stylized image of three human profiles facing to the right, stacked on top of each other.
June 22, 2017
Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-0002
Mcube Technology Co., Ltd. % Mr. Dave Yungvirt CEO Third Party Review Group, LLC The Old Station House 24 Lackawanna Place MILLBURN NJ 07041
Re: K171591
Trade/Device Name: CUBEScan" BioCon-900 (Bladder Volume Measurement System) Regulation Number: 21 CFR 892.1560 Regulation Name: Ultrasonic pulsed echo imaging system Regulatory Class: II Product Code: IYO, ITX Dated: May 28, 2017 Received: June 1, 2017
Dear Mr. Yungvirt:
We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and 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) that do not require approval of a premarket approval application (PMA). 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. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading.
If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to 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); medical device reporting (reporting of medical device-related adverse events) (21 CFR 803); 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.
1
If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please contact the Division of Industry and Consumer Education at its toll-free number (800) 638 2041 or (301) 796-7100 or at its Internet address
http://www.fda.gov/MedicalDevices/Resourcesfor You/Industry/default.htm. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR 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.
You may obtain other general information on your responsibilities under the Act from the Division of Industry and Consumer Education at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address
http://www.fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm.
Sincerely yours.
For
Robert Ochs, Ph.D. Director Division of Radiological Health Office of In Vitro Diagnostics and Radiological Health
Center for Devices and Radiological Health
Enclosure
2
DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration
Indication for Use
From Approved: OMB No. 0910-0120
Expiration Date: January 31, 2017
See PRA Statement below
510(k) Number (if known)
Device Name
CUBEScan™ BioCon-900 (Bladder Volume Measurement System)
Indications for use (Describe)
BioCon-900 is a B-mode pulsed-echo ultrasound device. The BioCon-900 projects ultrasonic energy through the lower of a patient to obtain images of the bladder to calculate the urine volume non-invasively. BioCon-900 is intended to be used by a qualified medical professional to non-invasively measure the urine in the bladder. Contraindications for the BioCon-900 are fetal use and use on pregnant patients.
Type of Use (Select one or both, as applicable)
2 Prescription Use (Part 21 CFR 801 Subpart D)
ロ Over-The-Counter Use (21 CFR 801 Subpart C)
CONTINUE ON A SEPARETE PAGE IF NEEDED.
This section applies only to requirements of the Paperwork Reduction Act of 1995.
DO NOT SEND YOUR COMPLETED FORM TO THE PRA STAFF EMAIL ADDRESS BELOW.
The burden time for this collection of information is estimated to average 79 hours per response, including the time to review instructions, search existing data sources, gather and maintain the data needed and complete and review the collection of information. Send comments regarding this burden estimate or any other aspect of this information collection, including suggestions for reducing this burden, to:
Department of Health and Human Services Food and Drug Administration Office of Chief Information Officer Paperwork Reduction Act (PRA) Staff PRAStaff@fda.hhs.gov
"An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB number."
FORM FDA 3881 (8/14)
Page 4 - 1
PSC Publishing Services (301) 443 6740 EF
3
Diagnostic Ultrasound Indications for Use Form
| System: | CUBEScan™ BioCon-900
Bladder Volume Measurement System | | | | | | | |
|-----------------------------|--------------------------------------------------------------------------------------------------|-------------------|---|-----|-----|------------------|-----------------------|------------------|
| Transducer: | BioCon-900 | | | | | | | |
| | Intended use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows: | | | | | | | |
| Clinical Application | | Mode of Operation | | | | | | |
| General
(Track 1 Only) | Specific
(Tracks 1 & 3) | B | M | PWD | CWD | Color
Doppler | Combined
(Specify) | Other* (Specify) |
| Ophthalmic | Ophthalmic | | | | | | | |
| | Fetal | | | | | | | |
| | Abdominal | N | | | | | | |
| | Intra-operative (Specify) | | | | | | | |
| | Intra-operative (Neuro) | | | | | | | |
| | Laparoscopic | | | | | | | |
| | Pediatric | | | | | | | |
| Fetal
Imaging
& Other | Small Organ (Specify) | | | | | | | |
| | Neonatal Cephalic | | | | | | | |
| | Adult Cephalic | | | | | | | |
| | Trans-rectal | | | | | | | |
| | Trans-vaginal | | | | | | | |
| | Trans-urethreal | | | | | | | |
| | Trans-esoph. (non-Card.) | | | | | | | |
| | Musculo-skeletal
(Conventional) | | | | | | | |
| | Musculo-skeletal
(Superficial) | | | | | | | |
| | Intravascular | | | | | | | |
| | Other (specify) | P | | | | | | |
| Cardiac | Cardiac Adult | | | | | | | |
| | Cardiac Pediatric | | | | | | | |
| | Intravascular (Cardiac) | | | | | | | |
| | Trans-esoph. (Cardiac) | | | | | | | |
| | Intra-cardiac | | | | | | | |
| | Other (specify) | | | | | | | |
| Peripheral
Vessel | Peripheral vessel | | | | | | | |
| | Other | | | | | | | |
N = new indication; P = previously cleared by FDA in K111021; E = added under this appendix
- Examples of other modes of operation may include: A-mode, Amplitude Doppler, 3-D Imaging, Harmonic Imaging, Tissue Motion Doppler, and Color Velocity Imaging
Prescription devices (Part 21 CFR 801.109)
4
510(k) Summary
This summary of 510(k) safety and effectiveness information is being submitted in accordance with requirements of 21 CFR 807.92.
1) SUBMITTER
| Submitter: | Mcube Technology Co., Ltd. |
|---|---|
| #803, 123 Bonghwasan-ro, | |
| Jungnang-gu, Seoul, Korea | |
| Contact Person: | Seung-Tai Kim |
| Director | |
| Phone: +82-(0)2-3421-7780 | |
| Fax: +82-(0)2-3421-7076 | |
| E-mail: mcube@mcubetech.co.kr | |
| Date Prepared: | Feb 15, 2016 |
2) DEVICE
| Trade Name(s): | CUBEScan™ BioCon-900 | |
|---|---|---|
| Common Name: | Bladder Volume Measurement System | |
| Classification: | II | |
| Classification Name(s): | Ultrasonic Pulsed Echo Imaging System | Diagnostic Ultrasound Transducer |
| Regulation Number: | 21 CFR 892.1560 | 21 CFR 892.1570 |
| Product Code: | IYO | ITX |
| Classification Panel: | Radiology |
3) PREDICATE DEVICE
| Predicate Devices: | Mcube Technology Co., Ltd.
CUBEScanTM BioCon-700 | K111021 |
|--------------------|-----------------------------------------------------|---------|
| | | |
4) DEVICE DESCRIPTION
CUBEScan™ BioCon-900 (bladder volume measurement system) is a safe and easy, non-invasive system to measure the bladder volume. CUBEScan™ BioCon-900 is a B-mode instrument, hand-held, wireless and battery-operated. A 3D-mechnical sector transducer provides cross-sectional images of the bladder from up to 12 scan planes and bladder volume is calculated based upon those images and displays 12 scan planes on a screen. Furthermore, a live image of the bladder during Pre-Scan makes it easier to detect the bladder before scanning. Measurements are transmitted to a personal computer running CubePro software via a wireless connection. CubePro allows the user to print measurements, archive data and so on.
5
5) INTENDED FOR USE/INDICATIONS FOR USE
BioCon-900 projects ultrasonic energy through the lower abdomen of a patient to obtain images of bladder to calculate the urine volume non-invasively.
6) COMPARISION OF CUBEscan™ BioCon-900 WITH THE PREDICATE DEVICES
The CUBEScan™ BioCon-900 is substantially equivalent to the currently marketed BioCon-700.
The subject and the predicate devices are based on the following same technological elements:
- · Intended use: Projection of ultrasonic energy into the abdomen of patients.
- Patient population and anatomical site
- Measurement of bladder volume
- · Accuracy of measurement
- Mode of operation
- · Transducer type, sector angle, number of element and number of scan planes
- · Acoustic output intensity
- Displays, portable, button controls, attached printer and PC software for data management
- Standards of safety, EMC, biocompatibility
The following technological differences exist between the CUBEScan™ BioCon-900 and predicate devices.
- Transducer resonant frequency
- Patient contact material
- Transducer diameter
- · Charger
- · Data Transmission tools(Touch screen operation and accessories)
- Input of information
- PC program version
6
7) Summary of Non-Clinical Testing Performed
The following performance data were provided in support of the substantial equivalence
Biocompatibility Testing
The biocompatibility test for CUBEScan™ BioCon-900 was conducted in accordance with ISO-10993 as recognized by FDA. The following tests performed:
-
Cytotoxicity Test (MEM Elution Test)
-
Maximization Sensation
-
Intracutaneous Reactivity
Electrical Safety and Electromagnetic Compatibility (EMC)
Electrical safety and EMC testing were conducted on the CUBEScan™ BioCon-900. The CUBEScan™ BioCon-900 complied with AAMI/ANSI ES 6060-1, IEC6060-1-2 for safety and EMC including battery, Ir communication, barcode and wireless charging.
Acoustic Output Testing
The acoustic output test for was CUBEScant™ BioCon-900 conducted in accordance with IEC60601-2-37.
Software Validation
Software Validation testing for CUBEScan™ BioCon-900 was conducted and documentation was provided as recommended "Guidance for the Content of Premarket Submissions for Software in Medical Devices".
Volume Measuring Testing
In order to demonstrate the accuracy of CUBEScan™ BioCon-900, a tissue-equivalent bladder phantom with a balloon which has a designated volume is used. The accuracy has been demonstrated by designated volume to the volume from CUBEScan™ BioCon-900.
Wireless Telecommunication & Charging
The CUBEScan 114 BioCon-900 is intended for use in an environment in which radiated RF disturbances are controlled. In order to demonstrate the safety of RF communications, Wireless Telecommunication Testing was conducted in accordance with 47 CFR FCC - Telecommunications, Chapter I - Federal Communications Commission, Subchapter A - General Part 15 - Radiofrequency Devices Subpart C section 15.207/15.209 and RF Exposure
8) Conclusions
In accordance with the Federal Food, Drug and Cosmetic Act, 21 CFR Part 807 and based on the information provided in this premarket notification. Mcube Technology Co., Ltd. concludes that the CUBEScan™ BioCon-900 is safe and effective and substantially equivalent to predicative devices as described herein.