(68 days)
K 002782
K 002782
No
The document describes a standard image processing and viewing workstation with optional image fusion capabilities. There is no mention of AI, ML, or any related technologies in the intended use, device description, or other sections.
No
The device is described as a workstation/server used to review, process, film, and store multi-modality images acquired from other diagnostic imaging systems, indicating a diagnostic rather than therapeutic purpose.
No
The "Intended Use / Indications for Use" states that the device reviews, processes, films, and stores images acquired from other diagnostic imaging systems. It does not acquire or analyze images for diagnostic purposes itself.
No
The device description explicitly lists hardware components such as a computer, keyboard, mouse, monitor, network interface, and optional storage devices and film digitizer.
Based on the provided information, the SCEPTRE-VS is not an IVD (In Vitro Diagnostic).
Here's why:
- Intended Use: The intended use clearly states that the device is for "review, process, film and store multi-modality images acquired from other diagnostic imaging systems or workstations." This describes a system for managing and displaying medical images, not for performing tests on biological samples.
- Device Description: The description details a computer workstation with peripherals used for storing, processing, viewing, and printing medical images. It does not mention any components or functions related to analyzing biological specimens.
- Input: The input is imaging data from various modalities (x-ray, MRI, CT, etc.), not biological samples.
IVD devices are used to examine specimens derived from the human body (like blood, urine, tissue) to provide information for diagnosis, monitoring, or screening. The SCEPTRE-VS operates on medical images, which are a different type of data.
N/A
Intended Use / Indications for Use
The intended use of the SCEPTRE-VS is to review, process, film and store multi-modality images acquired from other diagnostic imaging systems or workstations.
Product codes
90LLZ
Device Description
The SCEPTRE-VS is a workstation/server consisting of a computer, keyboard, mouse, monitor, network interface ;optional storage device(s) such as magneto-optical disk ,compact disk amd magnetic tape; and optional film digitizer. workstation, K 002782 The computer workstation is PC based utilizing the latest Intel Pentium technology. The operating system is Windows 2000/XP. The Sceptre-VS workstation is used to store, process, view and print diagnostic medical images from diagnostic imaging systems conforming to DICOM 3.0 including x-ray, MRI, CT, PET, Nuclear Medicine and Ultrasound. Several proprietary image formats can also be accomodated. The optional Fusion 7D fusion module can be used for fusion of 2 modalities such as CT/PET, MRI/PET to provide crossmodality comparison.
Mentions image processing
Yes
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
x-ray, MRI, CT, PET, Nuclear Medicine and Ultrasound. Several proprietary image formats can also be accomodated.
Anatomical Site
Not Found
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
Not Found
Key Metrics
Not Found
Predicate Device(s)
Nuclear-Diagnostics HERMES
Reference Device(s)
Not Found
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
510(k) Summary
Submitter Information: 1.
1/02/3/4
1.1. Submitter: Hitachi Medical Systems America, Inc. 1959 Summit Commerce Park Twinsburg, OH 44087 Phone: (847) 463-2001 FAX: (847) 463-2011
1.2. Manufacturing Facility: Hitachi Medical Systems America, Inc. 1959 Summit Commerce Park Twinsburg, OH 44087 Phone: (847) 463-2001 FAX: (847) 463-2011
1.3. Contact: Robert H. McCarthy
- Date: April 19, 2002 1.4.
2. Device Name
| 2.1. | Classification Name: | PACS (21CFR Section 892.2050) |
|---|---|---|
| Classification Number: | 90LLZ | |
| 2.2. | Trade/Proprietary Name: | SCEPTRE-VS |
| 2.3. | Predicate Device: | Nuclear-Diagnostics HERMES |
3. Device Description
3.1. Function
The SCEPTRE-VS is a workstation/server consisting of a computer, keyboard, mouse, monitor, network interface ;optional storage device(s) such as magneto-optical disk ,compact disk amd magnetic tape; and optional film digitizer.
workstation, K 002782
The computer workstation is PC based utilizing the latest Intel Pentium technology. The operating system is Windows 2000/XP.
The Sceptre-VS workstation is used to store, process, view and print diagnostic medical images from diagnostic imaging systems conforming to DICOM 3.0 including x-ray, MRI, CT, PET, Nuclear Medicine and
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Ultrasound. Several proprietary image formats can also be accomodated. The optional Fusion 7D fusion module can be used for fusion of 2 modalities such as CT/PET, MRI/PET to provide crossmodality comparison.
Device Intended Use: 4.
- 4.1. The intended use of the SCEPTRE-VS is to review, process, film and store multi-modality images acquired from other diagnostic imaging systems or workstations.
5. Device Technological Characteristics:
- 5.1. The characteristics of the Sceptre-VS workstation compare substantially with the Nuclear-Diagnostics Hermes Workstation predicate device, in both materials used, technology applied, and functional methodology, Differences of note do not affect safety and effectiveness of the device. intended use, or application methods. The device operates in a manner substantially equivalent to other cleared devices in this category, and performs as well as the predicate Hermes.
5.2. Safetv
The SCEPTRE-VS is a non-invasive device. It has been designed to comply with applicable safety standards and the applicable sections of 21CFR.
The results of the hazard analysis indicate that the device is of minor level of concern as defined in the "Guidance for the Content of Premarket Submissions for Software Contained in Medical Devices".
2
Image /page/2/Picture/0 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of a circular seal with the text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" around the perimeter. Inside the circle is an abstract symbol that resembles three human profiles facing right, with flowing lines beneath them.
DEPARTMENT OF HEALTH & HUMAN SERVICES
Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850
JUL = 2 2002
Mr. Robert H. MºCarthy Technical Director Hitachi Medical Systems America, Inc. 1959 Summit Commerce Park TWINSBURG OH 44087
Re: K021314
Trade/Device Name: Sceptre-VS Workstation Regulation Number: 21 CFR 892.2050 Regulation Name: Picture archiving and communications system
Regulatory Class: II Product Code: 90 LLZ Dated: April 24, 2002 Received: April 25, 2002
Dear Mr. M&Carthy:
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. Iisting of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration.
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); 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.
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This letter will allow you to begin marketing your device as described in your 510(k) 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 the market.
If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please contact the Office of Compliance at one of the following numbers, based on the regulation number at the top of this letter:
| 8xx.1xxx | (301) 594-4591 |
|---|---|
| 876.2xxx, 3xxx, 4xxx, 5xxx | (301) 594-4616 |
| 884.2xxx, 3xxx, 4xxx, 5xxx, 6xxx | (301) 594-4616 |
| 892.2xxx, 3xxx, 4xxx, 5xxx | (301) 594-4654 |
| Other | (301) 594-4692 |
Additionally, for questions on the promotion and advertising of your device, please contact the Office of Compliance at (301) 594-4639. Also, please note the regulation entitled. "Misbranding by reference to premarket notification" (21 CFR Part 807.97). Other general information on your responsibilities under the Act may be obtained from the Division of Small Manufacturers, 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/dsma/dsmamain.html.
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
Enclosure
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K02 1314 . 510(k) Number (if known): Sceptre-VS Device Name:
Indications for Use:
The intended use of the Sceptre-VS is to review, process, film and store multi-modality images acquired from other diagnostic imaging systems or workstations.
(PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NEEDED)
Concurrence of CDRH, Office of Device Evaluation (ODE)
David A. Lippman
(Division Sign-Off)
Division of Reproductive, Abdominal,
Division of Reproduc and Radiological De 510(k) Nun
Prescription Use
Over-the-Counter Use