ClearanceBrief
510(k) K896762 ยท GEX Powered Laser Surgical Instrument

SHARPLAN ND:YAG LASER FOR ARTHROSCOPY/MENISCECTOMY

ApplicantSharplan Lasers, Inc., Washington, D.C. DC, US
DecisionSubstantially Equivalent, Feb 16, 1990
ReceivedDec 1, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K896762

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.