# K960665: Echo-Com for MS-Windows Version 2.0

- Pathway: 510(k) (Traditional)
- Applicant: Cone Instruments, Inc.
- Decided: May 7, 1996 after 77 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: 1 generation back to K800766 (1980). 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)
- K800766: Echo-Comp, Digisonics, Inc. (1980) Summary page 1.

## Indications for use
The ECHO-COM for MS-Windows Version 2.0 cardiac software program is recommended for quantitative analysis of M-mode, B-mode, and Doppler ultrasound data. The system may be employed adjunctively in the performance of stress echocardiography in patients with suspected coronary artery disease either on-line by direct connection to the video signal output port of a suitable diagnostic ultrasound system or off-line by retrieving and processing previously stored data. The system permits the use of either standard or customized examination protocols, data analysis formulae, and report formats.

Source page: https://510kreport.com/device/K960665
Methodology: https://510kreport.com/methodology