ClearanceBrief
510(k) K073583 ยท GEX Powered Laser Surgical Instrument

MODIFICATION TO PALOMAR LUX1540 HANDPIECE

ApplicantPalomar Medical Products, Inc., Burlington MA, US
DecisionSubstantially Equivalent, Mar 26, 2008
ReceivedDec 20, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K073583

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.