# K981819: Angiolaz Ves-1CAM

- Pathway: 510(k) (Traditional)
- Applicant: Angiolaz, Inc.
- Decided: Aug 4, 1998 after 74 days
- Product code: FWF (Camera, Television, Endoscopic, Without Audio)
- Device class: 1
- Regulation: 21 CFR 878.4160
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
The VES-1CAM use is indicated when ever there is a need for the use of video in endoscopic procedure.

Source page: https://510kreport.com/device/K981819
Methodology: https://510kreport.com/methodology