ClearanceBrief
510(k) K935495 ยท GEX Powered Laser Surgical Instrument

PF404/409/410/411/416/418 W/PF319:0/319:1/319:2

ApplicantPerimed, Inc., Piscataway NJ, US
DecisionSubstantially Equivalent, Apr 18, 1994
ReceivedNov 15, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K935495

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.