LYRA G SERIES SURGICAL LASER SYSTEM (SL SERIES Q-SWITCHED ND:YAG CONFIGURATION)— 510(k) K010284

Substantially Equivalent

Laserscope

FDA 510(k) clearance K010284 for LYRA G SERIES SURGICAL LASER SYSTEM (SL SERIES Q-SWITCHED ND:YAG CONFIGURATION), Substantially Equivalent on 2001-05-01. Applicant: Laserscope.

Clearance details

Applicant: Laserscope
Product code: Code GEX
Advisory panel: General, Plastic Surgery
Date received: 2001-01-31
Decision date: 2001-05-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Jose, CA, US

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Adverse events under product code GEX

product code GEX

Death: 33
Injury: 3,045
Malfunction: 12,903
Other: 25
Total: 16,006

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.