# K100533: Vista Endoscope,89 CM, 56CM , Scout Blunt-Tipped Guide- 106 CM, 86 CM, 53 CM, Models FG0027, FG0031, FG0029, FG 0028,

- Pathway: 510(k) (Traditional)
- Applicant: Vibrynt, Inc.
- Decided: Feb 8, 2011 after 348 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: 3 generations back to K923982 (1993). 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)
- K053382: Laparo-Thoraco Videoscope XLTF-Vaw, Olympus Medical Systems Corporation (2006) Summary page 1.
- K051610: Hans Hermann Laparoscopes and Accessories, Hans Hermann GmbH (2005) Summary page 1.
- K063078: Microendoscope, Acclarent, Inc. (2006) Summary page 1.

## Most influential descendants
- K183264: Flex-THOR scope (2019), 0 descendants of its own

## Indications for use
The VISTA Endoscope and accessories are intended for use in providing access to, and visualization of, the thoracic and abdominal cavities, to allow for the performance of various diagnostic and therapeutic surgical procedures.

Source page: https://510kreport.com/device/K100533
Methodology: https://510kreport.com/methodology