ClearanceBrief
510(k) K974022 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

VAPR

ApplicantMitek Products, Westwood MA, US
DecisionSubstantially Equivalent, Jan 12, 1998
ReceivedOct 14, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K974022

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.