ClearanceBrief
510(k) K050047 ยท GEX Powered Laser Surgical Instrument

CUTERA OPTIONAL PULSED LIGHT HAND PIECE FAMILY

ApplicantCutera, Inc., Brisbane CA, US
DecisionSubstantially Equivalent, Mar 31, 2005
ReceivedJan 10, 2005
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K050047

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.