# K021290: Vista Visualization System, Model 9000, Vista Visualization System with Voice Activation and Pip, Model 9100

- Pathway: 510(k) (Abbreviated)
- Applicant: Vista Medical Technologies, Inc.
- Decided: Jun 28, 2002 after 66 days
- Product code: GCJ (Laparoscope, General & Plastic Surgery)
- Device class: 2
- Regulation: 21 CFR 876.1500
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K923160 (1992). 12 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 14 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K020301: Modification to Vista Stereoscope System, Vista Medical Technologies, Inc. (2002) Summary page 1.
- K973436: Vista Head Mounted Display, Vista Medical Technologies, Inc. (1997) Summary page 1.
- K991303: Vista Orpc with Infomatix Intraop Software, Vista Medical Technologies, Inc. (1999) Summary page 1.

## Most influential descendants
- K101810: 3DHJD Camera System Model (2010), 0 descendants of its own

## Indications for use
The Vista Visualization System is intended for use in endoscopic procedures and all types of video assisted procedures, including general endoscopic and laparoscopic, bariatric, thoracic, anterior and posterior spinal and as an aid in visualization of cardiac structures

Source page: https://510kreport.com/device/K021290
Methodology: https://510kreport.com/methodology