# K063600: Vista Avs

- Pathway: 510(k) (Traditional)
- Applicant: Summit Doppler Systems, Inc.
- Decided: Dec 19, 2006 after 15 days
- Product code: JAF (Monitor, Ultrasonic, Nonfetal)
- Device class: 2
- Regulation: 21 CFR 892.1540
- 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 K973562 (1998). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K973562: Imex Medical Systems, Inc. Imexlab 9100, Imex Medical Systems, Inc. (1998) Summary page 1.

## Most influential descendants
- K103693: Vantage Abi (2011), 0 descendants of its own

## Indications for use
Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:

Source page: https://510kreport.com/device/K063600
Methodology: https://510kreport.com/methodology