ClearanceBrief
510(k) K923605 ยท GEX Powered Laser Surgical Instrument

MODIFIED SHARPLAN 1041

ApplicantSharplan Lasers, Inc., Washington, D.C. DC, US
DecisionSubstantially Equivalent, Feb 23, 1994
ReceivedJul 10, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K923605

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.