# K981827: Ves 0281-M Complete Video Endoscopic Video System

- Pathway: 510(k) (Traditional)
- Applicant: Angiolaz, Inc.
- Decided: Jul 28, 1998 after 67 days
- Product code: FET (Endoscopic Video Imaging System/Component, Gastroenterology-Urology)
- 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
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. The FDA summary names no predicate by number.

## Indications for use
VES0281-m is for use as a visual aid for an endoscope when doing diagnostic evaluations or procedures.

Source page: https://510kreport.com/device/K981827
Methodology: https://510kreport.com/methodology