(23 days)
No
The summary describes a software application for viewing, analyzing, and measuring ultrasound volume data. There is no mention of AI, ML, or related concepts like deep learning, training sets, or performance metrics typically associated with AI/ML algorithms. The focus is on visualization and basic analysis tools.
No.
The device is a software application for displaying and analyzing ultrasound volume data, not for providing therapy.
Yes
The "Intended Use / Indications for Use" section states that the device is "designed to allow the user to observe images and perform analysis using the ultrasound volume data acquired with specified diagnostic ultrasound systems." This indicates its role in the diagnostic process.
Yes
The device is explicitly described as "standalone software" that is installed on standard laptops/PCs and processes data from external ultrasound systems. It does not include any hardware components of its own.
Based on the provided information, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- IVD definition: In vitro diagnostics are tests performed on samples taken from the human body, such as blood or tissue, to detect diseases, conditions, or infections. They are used to provide information for diagnosis, monitoring, or screening.
- Device function: The 5D Viewer software is designed to display, visualize, and analyze ultrasound volume data. Ultrasound is an in vivo imaging modality, meaning it creates images of structures inside the body without taking samples.
- Intended Use: The intended use clearly states it's for "display and 3D visualization of ultrasound volume data" and for "viewing, editing, measuring and storing of volume data" acquired from diagnostic ultrasound systems. This is focused on image processing and analysis, not on testing biological samples.
Therefore, since the device operates on imaging data acquired from within the body (in vivo) rather than on samples taken from the body (in vitro), it does not fit the definition of an In Vitro Diagnostic device.
N/A
Intended Use / Indications for Use
5D Viewer is a software application for the display and 3D visualization of ultrasound volume data derived from ultrasound system. It is designed to allow the user to observe images and perform analysis using the ultrasound volume data acquired with specified diagnostic ultrasound systems. It is intended to be used for viewing, editing, measuring and storing of volume data. Typical users of this system are trained professionals, including physicians, nurses, and technicians.
Product codes
LLZ
Device Description
5D Viewer is standalone software that can be installed in laptops/PCs with Microsoft Windows 7.
This product lets users use their computers to review, analyze, edit, and measure the volume data exported from ultrasound equipment via storage media such as USB drive.
Since this product reads 3D volume data, users can review the test results of patients more quickly and easily. This function allows them to check 3D image results without using an ultrasound system, helping them conduct more tests with the ultrasound system.
5D Viewer only supports the DICOM files containing the volume data created by Samsung Medison's Diagnostic Ultrasound Systems. In other words, you only use the volume data in DICOM files. 5D Viewer is not compatible with the DICOM files from third parties.
Main operational functions
- Display and edit volume data set
- · Save data (video and volume data)
- · Support simple caliper (Distance, Ellipse, or 3 Distance Volume)
Functions that require a USB-type dongle
- HDVI
- · 5D Heart
5D Viewer uses the volume data of Samsung Medison's WS80A, and HS70A Ultrasound systems. The Volume Data contains the raw data obtained during the scan as well as the information required for rendering (e.g., Geometry, View mode, etc.). The patient information is not relevant to the rendering, so it is not included in the Volume Data.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Ultrasound
Anatomical Site
Not Found
Indicated Patient Age Range
Not Found
Intended User / Care Setting
Typical users of this system are trained professionals, including physicians, nurses, and technicians.
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 tests were conducted to conform to applicable voluntary standards: IEC 62304 Medical device software Software life-cycle processes, ISO 14971 Medical devices Application of risk management to medical devices (ISO 14971:2007, Corrected version 2007-10-01), HIPAA COMPLIANCE 5D Viewer is in compliance with the Health Insurance Portability and Accountability Act of 1996 (HIPAA), and SAMSUNG MEDISON Software Development Procedure (DXQ2-0030K).
Clinical studies were not required to support substantial equivalence.
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
Not Found
Predicate Device(s)
Reference Device(s)
WS80A Diagnostic Utrasound System (K143089)
Predetermined Change Control Plan (PCCP) - All Relevant Information
Not Found
§ 892.2050 Medical image management and processing system.
(a)
Identification. A medical image management and processing system is a device that provides one or more capabilities relating to the review and digital processing of medical images for the purposes of interpretation by a trained practitioner of disease detection, diagnosis, or patient management. The software components may provide advanced or complex image processing functions for image manipulation, enhancement, or quantification that are intended for use in the interpretation and analysis of medical images. Advanced image manipulation functions may include image segmentation, multimodality image registration, or 3D visualization. Complex quantitative functions may include semi-automated measurements or time-series measurements.(b)
Classification. Class II (special controls; voluntary standards—Digital Imaging and Communications in Medicine (DICOM) Std., Joint Photographic Experts Group (JPEG) Std., Society of Motion Picture and Television Engineers (SMPTE) Test Pattern).
0
Image /page/0/Picture/1 description: The image shows the logo for the Department of Health & Human Services - USA. The logo consists of a circular seal with the text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" arranged around the perimeter. Inside the circle is a stylized graphic of three human profiles facing to the right, overlapping each other to create a sense of depth and connection. The profiles are rendered in a simple, bold line style.
Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-0002
August 10, 2016
Samsung Medison Co., Ltd. % Mr. Mark Job Responsible Third Party Official Regulatory Technology Services LLC 1394 25th Street, NW BUFFALO MN 55313
Re: K161955
Trade/Device Name: 5D Viewer Regulation Number: 21 CFR 892.2050 Regulation Name: Picture archiving and communications system Regulatory Class: II Product Code: LLZ Dated: July 14, 2016 Received: July 18, 2016
Dear Mr. Job:
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.
Michael D'Hara
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
Indications for Use
510(k) Number (if known) K161955
Device Name 5D Viewer
Indications for Use (Describe)
5D Viewer is a software application for the display and 3D visualization of ultrasound volume data derived from ultrasound system. It is designed to allow the user to observe images and perform analysis using the ultrasound volume data acquired with specified diagnostic ultrasound systems. It is intended to be used for viewing, editing, measuring and storing of volume data. Typical users of this system are trained professionals, including physicians, nurses, and technicians.
| Type of Use (Select one or both, as applicable) | |
|---|---|
| ☒ Prescription Use (Part 21 CFR 801 Subpart D) | ☐ Over-The-Counter Use (21 CFR 801 Subpart C) |
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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:
SAMSUNG MEDISON CO., LTD. 42, Teheran-ro 108-gil, Gangnam-gu, Seoul, Korea
Contact Person:
Kyeong-Mi, Park Regulatory Affairs Manager
Telephone: 82.2.2194.1373 Facsimile: 82.2.556.3974
Data Prepared: June 3, 2016
2. Name of the device:
Common/Usual Name: Picture Archiving Communications System Proprietary Name: 5D Viewer Classification Names: FR Number Product Code Picture Archiving Communications System 892.2050 LLZ
3. Identification of the predicate or legally marketed device:
- -3D/5D Viewer (K151808)
- WS80A Diagnostic Ultrasound System (K153529) -
- RS80A Diagnostic Ultrasound System (K151663) -
4
4. Device Description:
5D Viewer is standalone software that can be installed in laptops/PCs with Microsoft Windows 7.
This product lets users use their computers to review, analyze, edit, and measure the volume data exported from ultrasound equipment via storage media such as USB drive.
Since this product reads 3D volume data, users can review the test results of patients more quickly and easily. This function allows them to check 3D image results without using an ultrasound system, helping them conduct more tests with the ultrasound system.
5D Viewer only supports the DICOM files containing the volume data created by Samsung Medison's Diagnostic Ultrasound Systems. In other words, you only use the volume data in DICOM files. 5D Viewer is not compatible with the DICOM files from third parties.
Main operational functions
- Display and edit volume data set
- · Save data (video and volume data)
- · Support simple caliper (Distance, Ellipse, or 3 Distance Volume)
Functions that require a USB-type dongle
- HDVI
- · 5D Heart
5D Viewer uses the volume data of Samsung Medison's WS80A, and HS70A Ultrasound systems. The Volume Data contains the raw data obtained during the scan as well as the information required for rendering (e.g., Geometry, View mode, etc.). The patient information is not relevant to the rendering, so it is not included in the Volume Data.
5. Intended Uses:
5D Viewer is a software application for the display and 3D visualization of Ultrasound volume data derived from Ultrasound system. It is designed to allow the user to observe images and perform analysis using the volume data acquired with specified diagnostic ultrasound systems. It is intended to be used for viewing. analyzing, editing, measuring and storing of volume data.
6. Technological Characteristics:
5D Viewer is substantially equivalent with respect to safety, effectiveness, and functionality to the 3D/5D Viewer (K151808), WS80A Diagnostic Utrasound System (K143089) and RS80A Diagnostic Ultrasound
5
System (K151663).
The device is a software application and does not contact the patient, nor does it control any life sustaining devices. A physician, providing ample opportunity for competent human intervention interprets volume data being displayed. It is designed to allow the user to observe images and perform analysis using the volume data acquired with specified diagnostic ultrasound systems. It is intended to be used for viewing, analyzing, editing, measuring and storing of volume data.
These are described in detail in the technological characteristics comparison table as below.
| Feature | Subject Device | The Primary predicate devices | The predicate devices | |
|---|---|---|---|---|
| 5D Viewer | 3D/5D Viewer | |||
| (K151808) | WS80A | |||
| (K153529) | RS80A | |||
| (K151663) | ||||
| Computer | ||||
| Operating System |
- Windows 7 | Yes | Yes | Not applicable | Not applicable |
| Opening and
saving files | | | | |
| - *.mvl | Yes | Yes | Yes | Yes |
| - *.sty | Yes | Yes | Yes | Yes |
| - *.dcm | Yes | No | Yes | Yes |
| - MPR | | | | |
| Slub 3D | Yes | Yes | Yes | Yes |
| Accept ROI | Yes | Yes | Yes | Yes |
| FAD | Yes | Yes | Yes | Yes |
| Curved ROI | Yes | Yes | Yes | Yes |
| - Mirror View | Yes | Yes | Yes | Yes |
| - MagiCut | | | | |
| Smooth Cut | Yes | Yes | Yes | Yes |
| - Volume Slice | Yes | Yes | Yes | Yes |
| - MSV | Yes | Yes | Yes | Yes |
| - Oblique View | Yes | Yes | Yes | Yes |
| - Volume CT | Yes | Yes | Yes | Yes |
| - VOCAL | Yes | Yes | Yes | Yes |
| - XI VOCAL | Yes | Yes | Yes | Yes |
| - Cine View | | | | |
| 3D Cine | Yes | Yes | Yes | Yes |
| 4D Cine | Yes | Yes | Yes | Yes |
| - 5D Functions | | | | |
| 5D NT | Yes | Yes | Yes | No |
| 5D CNS+
(old name:
5D CNS) | Yes | Yes | Yes | No |
| 5D Follicle | Yes | Yes | Yes | No |
| 5D LB | Yes | Yes | Yes | No |
| Feature | Subject Device | The Primary predicate devices | The predicate devices | |
| | 5D Viewer | 3D/5D Viewer
(K151808) | WS80A
(K153529) | RS80A
(K151663) |
| 5D Heart | Yes | Yes | Yes | No |
| 5D Limb Vol | Yes | No | Yes | No |
| - Measurement | | | | |
| Distance | Yes | Yes | Yes | Yes |
| Ellipse 3 | Yes | Yes | Yes | Yes |
| Distance | Yes | Yes | Yes | Yes |
| - Volume | | | | |
| - Render Setup | | | | |
| functions | | | | |
| Realistic | Yes | Yes | Yes | Yes |
| Vue VSI | Yes | Yes | Yes | Yes |
| ClearVision | Yes | No | Yes | Yes |
| Crystal Vue | Yes | No | Yes | No |
| Natural Vue | Yes | No | No | No |
| - Post Processing | | | | |
| functions | | | | |
| Post Gain | Yes | Yes | Yes | Yes |
| Clear SFVI | Yes | Yes | Yes | Yes |
| Detailed SFVI | Yes | Yes | Yes | Yes |
| HDVI | Yes | Yes | Yes | Yes |
| - Chroma map | Yes | Yes | Yes | Yes |
| function | | | | |
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| 5D Viewer | Addition of V1.01 | Remarks | ||||
|---|---|---|---|---|---|---|
| Model Name | • Change of model name in the V1.01 | |||||
| (3D/5D Viewer → 5DViewer) | ||||||
| SW Features | • Adding the predicate S/W features | |||||
| : ClearVision, Natural Vue, Crystal | ||||||
| Vue and 5D Limb Vol. | ||||||
| • Improving the S/W feature that | ||||||
| waspreviously cleared in 3D/5D Viewer | ||||||
| (K151808) | ||||||
| : 5D CNS+ | ||||||
| • Changing the S/W feature's name |
- 5D CNS → 5D CNS+ | Description of S/W Features
• ClearVision: It provides the function
of removing the noise in images and intensifies
boundary lines to make more vivid.
• Natural Vue: It shows the reflected light
onthe object surface by the light source to
improve realism and representation of shape
• Crystal Vue: This feature is the volume
rendering technology that visualizing
interior and exterior structures of 3D
volume data.
• 5D Limb Vol: This feature allows you to
detect fractional limb contour and to
measure semi-automatically the volume | | | | |
| | SW Features The previously
cleared SW
Features ClearVision K153529 | | | | | |
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| 5D Viewer | Addition of V1.01 | Remarks | |
|---|---|---|---|
| Natural Vue | K151663 | fractional limb. | |
| Crystal Vue | K153529 | ||
| 5D Limb Vol | K153529 |
7. A brief discussion of the non-clinical and clinical tests conducted on the subject device
The device has been evaluated to conform to applicable voluntary standards.
- IEC 62304 Medical device software Software life-cycle processes
- ISO 14971 Medical devices Application of risk management to medical devices (ISO 14971:2007, Corrected version 2007-10-01)
- HIPAA COMPLIANCE 5D Viewer is in compliance with the Health Insurance Portability and Accountability Act of 1996 (HIPAA).
- SAMSUNG MEDISON Software Development Procedure (DXQ2-0030K)
Summary of Clinical Tests:
Not applicable. The subject of this submission, 5D Viewer, did not require clinical studies to support substantial equivalence.
8. Conclusion
SAMSUNG MEDISON CO., LTD. considers the 5D Viewer to be as safe, as effective, and performance is substantially equivalent to the predicate devices.
- The 510(k) Pre-Market Notification for the 5D Viewer contains adequate information and data to enable FDA - CDRH to determine substantial equivalence to the predicate device.
- The device will be manufactured in accordance with the voluntary standards listed in the enclosed voluntary standard survey.
- The submission contains the results of a hazard analysis and the potential hazards have been classified as Minor.