ClearanceBrief
510(k) K837342 ยท

SHARPLAN 721 CO2 SURGICAL LASER

ApplicantLaser Industries , Ltd., Tel Aviv, IL
DecisionSubstantially Equivalent, May 18, 1983
ReceivedMar 8, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K837342

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.