ClearanceBrief
510(k) K955662 ยท GEX Powered Laser Surgical Instrument

CANDELA Q-SWITCHED ALEXANDRITE LASERS

ApplicantCandela Laser Corp., Wayland MA, US
DecisionSubstantially Equivalent, Jun 14, 1996
ReceivedDec 12, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K955662

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.