ClearanceBrief
510(k) K003886 ยท GEX Powered Laser Surgical Instrument

PALOMAR SPALIGHT PULSED LIGHT SYSTEM

ApplicantPalomar Medical Technologies, Inc., Cary NC, US
DecisionSubstantially Equivalent, Mar 1, 2001
ReceivedDec 18, 2000
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K003886

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.