ClearanceBrief
510(k) K900592 ยท GEX Powered Laser Surgical Instrument

SHARPLAN MODEL 1055 SEALED CO2 SURGICAL LASER

ApplicantSharplan Lasers, Inc., Washington, D.C. DC, US
DecisionSubstantially Equivalent, Mar 27, 1990
ReceivedFeb 7, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K900592

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.