# K963044: Endobeam

- Pathway: 510(k) (Traditional)
- Applicant: Corin USA
- Decided: Sep 20, 1996 after 46 days
- Product code: GCT (Light Source, Endoscope, Xenon Arc)
- 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 its predicate without a number.
- (no number) Autobrite: named in the summary without a submission number

## Indications for use
Endoscopic light source to provide illumination for fibre optic endoscopy to joint cavities and abdominal space.

Source page: https://510kreport.com/device/K963044
Methodology: https://510kreport.com/methodology