ClearanceBrief
510(k) K033172 ยท GEX Powered Laser Surgical Instrument

CANDELA GENTLEYAG FAMILY OF LASER SYSTEMS

ApplicantCandela Corp., Wayland MA, US
DecisionSubstantially Equivalent, Oct 30, 2003
ReceivedSep 30, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K033172

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.