510(k) K990665— BQ/BM INTEGRATED LASER DELIVERY SYSTEM

Substantially Equivalent

American Laser Corp.

Clearance details

Applicant: American Laser Corp.
Product code: Code HQF
Advisory panel: Ophthalmic
Date received: 1999-03-02
Decision date: 1999-05-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

Adverse events under product code HQF

product code HQF

Injury: 166
Other: 1
Total: 167

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.