# K992447: 50 W Metal Halide Illuminator, Ves 0501.

- Pathway: 510(k) (Traditional)
- Applicant: Angiolaz, Inc.
- Decided: Oct 20, 1999 after 90 days
- Product code: FCW (Light Source, Fiberoptic, Routine)
- 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. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
The 50 W Metal Halide Illuminator has indicated use in the following situations: There is a requirement for illuminating medical headlamps. There is a requirement for fiber-optic illumination for endoscopy applications. There is a requirement to use video as a visual aid or a method of recording or both. There is a requirement for any or all of the above at the same time.

Source page: https://510kreport.com/device/K992447
Methodology: https://510kreport.com/methodology