LIGHTLAS 577 MEDICAL OPTICAL PUMPED SEMICONDUCTOR LASER— 510(k) K091981

Substantially Equivalent

Lightmed Corp.

FDA 510(k) clearance K091981 for LIGHTLAS 577 MEDICAL OPTICAL PUMPED SEMICONDUCTOR LASER, Substantially Equivalent on 2009-09-28. Applicant: Lightmed Corp..

Clearance details

Applicant: Lightmed Corp.
Product code: Code HQF
Advisory panel: Ophthalmic
Date received: 2009-07-01
Decision date: 2009-09-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Taipei, TW

Download summary PDF View on FDA.gov ↗

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.