# K981821: Ves 3001/2 Dual Output Video Illuminator

- Pathway: 510(k) (Traditional)
- Applicant: Angiolaz, Inc.
- Decided: Jul 29, 1998 after 68 days
- Product code: FSS (Light, Surgical, Floor Standing)
- Device class: 2
- Regulation: 21 CFR 878.4580
- 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 3001/w use is indicated in the following situations: Whenever there is a need for head lamp illumination of the fiber-optic type When ever there is a need for a fiber-optic illuminator for an endoscope When ever there is a need to use video either as a visual aid for as a method of recording or both. When ever there is a requirement for any or all of the above at the same time.

Source page: https://510kreport.com/device/K981821
Methodology: https://510kreport.com/methodology