ClearanceBrief
510(k) K896847 ยท GEX Powered Laser Surgical Instrument

SHARPLAN 1030 SEALED CO2 SURGICAL LASER SYSTEM

ApplicantSharplan Lasers, Inc., Washington, D.C. DC, US
DecisionSubstantially Equivalent, Jan 24, 1990
ReceivedDec 5, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K896847

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.