# K992259: Echocardiography System Series 95000

- Pathway: 510(k) (Traditional)
- Applicant: Camtronics, Ltd.
- Decided: Sep 8, 1999 after 64 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: 3 generations back to K950279 (1995). 3 ancestors in all.
16 later devices descend from it; 3 cite it directly.
0 of 20 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K980060: Echolink, Mpacs, LLC (1998) Summary page 1.

## Most influential descendants
- K041029: Kinetdx (2004), 13 descendants of its own
- K053133: Syngo Dynamics, Version 5.0 (2005), 7 descendants of its own
- K111319: Ibis Explorer and Markup Software (2011), 6 descendants of its own
- K122205: EXINI (2012), 5 descendants of its own
- K050943: GE Viewpoint (2005), 3 descendants of its own

## Indications for use
A digital image capture, storage, and review system for echocardiography.

Source page: https://510kreport.com/device/K992259
Methodology: https://510kreport.com/methodology