(84 days)
Not Found
No
The summary describes a standard PACS system for image storage, retrieval, and display, with no mention of AI or ML capabilities.
No
The device is described as a radiology suite providing access, storage, and display of clinical reports and images. It does not mention any therapeutic function.
Yes
The device provides access to and displays clinical images (CR, CT, MR, XA, SC, US, NM, PET, and RT) for any human anatomy, and facilitates clinical reports, which are all integral to the diagnostic process.
No
The device description mentions adherence to standards like UL 187 and IEC 601-1, which are typically related to the safety and performance of electrical and mechanical hardware components, suggesting the device includes more than just software.
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, urine, or tissue, to detect diseases, conditions, or infections. They are used to provide information for diagnosis, monitoring, or screening.
- Device Function: The JPACS radiology suite is described as a system for accessing, storing, distributing, and displaying clinical reports and images generated by various medical imaging modalities (CR, CT, MR, etc.). It also facilitates the generation and distribution of clinical reports.
- Lack of Biological Sample Analysis: The description does not mention any analysis of biological samples. The device works with images and reports generated from imaging procedures performed on the human body.
Therefore, the JPACS radiology suite falls under the category of medical imaging software and systems, not in vitro diagnostics.
N/A
Intended Use / Indications for Use
The JPACS radiology suite is intended to provide access to clinical reports and images via computer networks. It is also intended to provide short, medium and long range storage of clinical images from any authorized workstation within an intranet or over the Internet. The full feature imaging suite can be used for in-house image distribution, on-call teleradiology, and advance visual display features. The JPACS radiology suite also includes functionality for generation and distribution of clinical reports.
The JPACS radiology suite provides access to clinical reports and images via computer networks. Given the following information objects, the JPACS radiology suite may be used on any part of the human anatomy: CR, CT, MR, XA, SC, US, NM, PET, and RT. The suite also provides short, medium, and long term storage of these clinical images from any authorized workstation within an intranet or over the Internet. The full feature imaging suite can be used for in-house image distribution, on-call teleradiology, and advance visual display features. The JPACS radiology suite also includes functionality for generation and distribution of clinical reports.
Product codes (comma separated list FDA assigned to the subject device)
90 LLZ, 90 LMD
Device Description
The JPACS radiology suite is intended to provide access to clinical reports and images via computer networks. It is also intended to provide short, medium and long range storage of clinical images from any authorized workstation within an intranet or over the Internet. The full feature imaging suite can be used for in-house image distribution, on-call teleradiology, and advance visual display features. The JPACS radiology suite also includes functionality for generation and distribution of clinical reports. Picker adheres to FDA 21 CFR 820 and voluntary standards for safety and effectiveness (UL 187) all of which mandate that components are tested to minimize hazards (electrical, mechanical, and radiation). In addition, the system is designed to conform to IEC 601-1. The subject device has the same technological characteristics as a legally marketed predicate device. Specifically, the features, specifications, materials, and mode of operation are equivalent. External communication uses DICOM V. 3.0 NEMA Standards Publication Parts PS3.1 through PS3.13, dated 1996.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
CR, CT, MR, XA, SC, US, NM, PET, and RT.
Anatomical Site
any part of the human anatomy
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)
Not Found
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
§ 892.2020 Medical image communications device.
(a)
Identification. A medical image communications device provides electronic transfer of medical image data between medical devices. It may include a physical communications medium, modems, and interfaces. It may provide simple image review software functionality for medical image processing and manipulation, such as grayscale window and level, zoom and pan, user delineated geometric measurements, compression, or user added image annotations. The device does not perform advanced image processing or complex quantitative functions. This does not include electronic transfer of medical image software functions.(b)
Classification. Class I (general controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to § 892.9.
0
3 1898 JUN
JPACS SUBSTANTIAL EQUIVALENCE SUMMARY K980918, page 1 OF 3
The following information is being submitted in accordance with 21 CFR 807.92(a) and in the order specified in that section.
(1) The submitter's name, address, telephone number, a contact person, and the date the summary was prepared;
| Submitter: | Picker International, Inc.
595 miner Road
Highland Heights, Ohio 44143
(440)473-3000 |
|------------|---------------------------------------------------------------------------------------------------------------------|
| Contact: | Robert L. Turocy
Picker International, Inc.
595 Miner Road
Highland Heights, Ohio 44143
(440) 473-3528 |
Date of Summary: March 26, 1998
(2) The name of the device, including the trade name or proprietary name if applicable, the common or usual name, and the classification name, if known;
| Device Name
| (Proprietary Name): | JPACS |
|---|---|
| Classification Name: | Picture Archiving & Communication System |
| Common Name: | Picture Archiving & Communication System |
The FDA has classified the JPACS as a Class II device, "Unclassified" Procode 90 LLZ based on recommendation of the Radiology Devices Panel.
(3) An identification of the legally marketed device to which the submitter claims equivalence. A legally marketed device to which a new device may be compared for a determination regarding substantial equivalence is a device that was legally marketed prior to May 28, 1976, or a device which has been reclassified from Class III to Class II or I the predicate) or a device which has been found to be substantially equivalent through the 510(k) Premarket Notification process.
Picker claims equivalence to the legally marketed device identified as the Medisurf manufactured by Algotec Systems Ltd. granted marketing permission in Document Control Number K971347.
1
JPACS SUBSTANTIAL EQUIVALENCE SUMMARY K980918, page 2 OF 3
(4) A description of the device that is the subject of the Premarket Notification submission, such as might be found in the labeling or promotional material for the device, including an explanation of how the device functions, the scientific concepts that form the basis for the device, and the significant physical and performance characteristics of the device such as device design, material used, and physical properties;
The JPACS radiology suite is intended to provide access to clinical reports and images via computer networks. It is also intended to provide short, medium and long range storage of clinical images from any authorized workstation within an intranet or over the Internet. The full feature imaging suite can be used for in-house image distribution, on-call teleradiology, and advance visual display features. The JPACS radiology suite also includes functionality for generation and distribution of clinical reports. Picker adheres to FDA 21 CFR 820 and voluntary standards for safety and effectiveness (UL 187) all of which mandate that components are tested to minimize hazards (electrical, mechanical, and radiation). In addition, the system is designed to conform to IEC 601-1. The subject device has the same technological characteristics as a legally marketed predicate device. Specifically, the features, specifications, materials, and mode of operation are equivalent. External communication uses DICOM V. 3.0 NEMA Standards Publication Parts PS3.1 through PS3.13, dated 1996.
(5) A statement of the intended use of the device that is subject of the Premarket Notification submission, including a general description of the diseases or conditions that the device will diagnose, treat, prevent, cure, or will mitigate, including a description, where appropriate, of the patient population for which the device is intended. If the indication statements are different from those of the legally marketed device identified in paragraph (a)(3) of this section, the 510(k) summary shall contain an explanation as to why the differences are not critical to the intended therapeutic, diagnostic, prosthetic, or surgical use of the device, and why the differences do not affect the safety and effectiveness of the device when used as labeled: and
Intended Use Statement: The JPACS radiology suite is intended to provide access to clinical reports and images via computer networks. It is also intended to provide short, medium and long range storage of clinical images from any authorized workstation within an intranet or over the Internet. The full feature imaging suite can be used for in-house image distribution, on-call teleradiology, and advance visual display features. The JPACS radiology suite also includes functionality for generation and distribution of clinical reports.
2
JPACS SUBSTANTIAL EQUIVALENCE SUMMARY K980918, page 3 OF 3
(6) If the device has the same technological characteristics (i.e., design, material, chemical composition, energy source) as the predicate device identified in paragraph (a)(3) of this section, a summary of the technological characteristics of the new device in comparison to those of the predicate device. If the device has different technological characteristics from the predicate device, a summary of how the technological characteristics of the device compare to a legally marketed device identified in paragraph (a)(3) of this section.
Claims: The JPACS is a comparable type and substantially equivalent to legally marketed devices. The intended use of the JPACS is the same as legally marketed device Medisurf manufactured by Algotec Systems Ltd. granted marketing permission and no new questions of safety or effectiveness are raised with the JPACS. The subject device has the same technological characteristics as a legally marketed predicate device. Specifically, the features, specifications, materials, mode of operation are equivalent.
3
DEPARTMENT OF HEALTH & HUMAN SERVICES. USA
Public Health Service
Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850
3 1000 IN
Robert L. Turocy Regulatory Affairs & Compliance Manager Picker International, Inc. 595 Miner Road Highland Heights, Ohio 44143
K980918 Re:
JPACS Dated: March 6, 1998 Received: March 11, 1998 Regulatory class: Unclassified Procode: 90 LMD
Dear Mr. Turocy:
We have reviewed your Section 510/k) 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 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.
If your device is classified (see above) into either class II (Special Controls) or class III (Premarket Approval), it may be subject to such additional controls. Existing major regulations affecting your device can be found in the Code of Fecteral Regulations, Title 21, Parts 800 to 895. A substantially equivalent determination assumes compliance with the Current Good Manufacturing Practice requirements, as set forth in the Quality System Regulation (OS) for Medical Devices: General regulation (21 CFR Part 820) and that, through periodic QS inspections, the Food and Drug Administration (FDA) will verify such assumptions. Failure to comply with the GMP regulation may result in regulatory action. In addition, FDA may publish further announcements concerning your device in the Federal Register. Please note: this response to your premarket notification submission does not affect any obligation you might have under sections 542 of the Act for devices under the Electronic Product Radiation Control provisions, or other Federal laws or regulations.
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 and additionally 809.10 for in vitro diagnostic devices), please contact the Office of Compliance at (301) 594-4613. 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 807.97). Other general information on your responsibilities under the Act may be obtained from the Division of Small Manufacturers Assistance at its toll-free number (800) 638-2041 or (301) 443-6597 or at its Internet address "http://www.fda.gov/odrh/dsmaldsmamain.html".
Sincerely yours,
Kilian Yin
Lillian Yin, Ph.D Director, Division of Reproductive Abdominal, Ear. Nose and Throa and Radiological Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
4
page 1 of 1
510(K) Number (if known): K98 ଫ 9 / 8
Device Name: JPACS
Indications for Use:
The JPACS radiology suite provides access to clinical reports and images via computer networks. Given the following information objects, the JPACS radiology suite may be used on any part of the human anatomy: CR, CT, MR, XA, SC, US, NM, PET, and RT. The suite also provides short, medium, and long term storage of these clinical images from any authorized workstation within an intranet or over the Internet. The full feature imaging suite can be used for in-house image distribution, on-call teleradiology, and advance visual display features. The JPACS radiology suite also includes functionality for generation and distribution of clinical reports.
(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)
Gind A. Segger
(Division Sign-Off)
Division of Reproductive, Abdominal, ENT, and Radiological Devices
510(k) Number K980918
Prescription Use (Per 21 CFR 801.109)
OR
Over-The Counter Use
(Optional Format 1-2-96)