ClearanceBrief
510(k) K883541 ยท GEX Powered Laser Surgical Instrument

METALASER VASCULASE

ApplicantMetatech Corp., Pleasanton CA, US
DecisionSubstantially Equivalent, Nov 4, 1988
ReceivedAug 19, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K883541

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.