ClearanceBrief
510(k) K782030 ยท GEX Powered Laser Surgical Instrument

LASER SYSTEM, SHARPLAN 791/HE, CO2

ApplicantLaser Industries , Ltd., Mchenry IL, US
DecisionSubstantially Equivalent, Jan 22, 1979
ReceivedDec 5, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K782030

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.