ClearanceBrief
510(k) K920062 ยท GEX Powered Laser Surgical Instrument

CANDELA PLTL-1 LASER SYSTEM: PIGMENTED LESION LAS.

ApplicantCandela Laser Corp., Wayland MA, US
DecisionSubstantially Equivalent, Jun 5, 1992
ReceivedJan 7, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K920062

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.