# K990665: BQ/BM Integrated Laser Delivery System

- Pathway: 510(k) (Traditional)
- Applicant: American Laser Corp.
- Decided: May 17, 1999 after 76 days
- Product code: HQF (Laser, Ophthalmic)
- Device class: 2
- Regulation: 21 CFR 886.4390
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K973220 (1997). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K973220: Rodenstock Laser Slitlamp, G. Rodenstock Instrumente GmbH (1997) Summary page 1.
- (no number) Zeiss 130 SL Laser Slit Lamp: named in the summary without a submission number

## Indications for use
1. RETINAL PHOTOCOAGULATION 2. TRABECULOPLASTY

Source page: https://510kreport.com/device/K990665
Methodology: https://510kreport.com/methodology