# K955708: Compumed Dicon Client

- Pathway: 510(k) (Traditional)
- Applicant: Compumed, Inc.
- Decided: Mar 1, 1996 after 78 days
- Product code: LMD (System, Digital Image Communications, Radiological)
- Device class: 1
- Regulation: 21 CFR 892.2020
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) CompuMed PC Teleradiology product: named in the summary without a submission number
- (no number) Dejarnette Teleshare: named in the summary without a submission number
- (no number) Line Imaging WinRad: named in the summary without a submission number
- (no number) SIENET DRC (MagicView workstation): named in the summary without a submission number

## Indications for use
This premarket notification covers the LAN and WAN teleradiology concept (transmission), and study information distribution functions. The CompuMed DICOM client is a viewing station manufactured by CompuMed, Inc. The CompuMed DICOM client is an on-site (LAN) or off-site (WAN or dial up) station for viewing patient information and images and reporting. It supports industry standard information transmission and communication protocols.

Source page: https://510kreport.com/device/K955708
Methodology: https://510kreport.com/methodology