# K961451: Dicomnet

- Pathway: 510(k) (Traditional)
- Applicant: Lockheed Martin Communications Systems
- Decided: Jul 3, 1996 after 78 days
- Product code: IZI (System, X-Ray, Angiographic)
- Device class: 2
- Regulation: 21 CFR 892.1600
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K943355 (1994). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K943355: Gemnet, GE Medical Systems (1994) Summary page 2.

## Indications for use
DicomNet is intended to be used for storing and displaying digital images acquired and stored by digital imaging systems on DICOM interchange media. DicomNet reviews images directly from the DICOM storage media (CD-Recordable disks) and can store the images in an archive manager for review on any of the network review stations. The system stores unaltered/uncompressed computer digital data.

Source page: https://510kreport.com/device/K961451
Methodology: https://510kreport.com/methodology