# K070089: Syntermed Live

- Pathway: 510(k) (Traditional)
- Applicant: Syntermed, Inc.
- Decided: Mar 2, 2007 after 52 days
- Product code: LLZ (System, Image Processing, Radiological)
- Device class: 2
- Regulation: 21 CFR 892.2050
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K942120 (1994). 7 ancestors in all.
No later device cites it as a predicate yet.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K042313: Integradweb MPR/Mip, Dynamic Imaging, Inc. (2004) Summary page 1.

## Indications for use
The Syntermed Live TM software program should be used for the transfer of medical images and data to a secure server for storage where it can subsequently be accessed, displayed, and processed on any PC connected to the Internet using either proprietary software applications, a DICOM Viewer, or a Web Browser.

Source page: https://510kreport.com/device/K070089
Methodology: https://510kreport.com/methodology