ClearanceBrief
510(k) K780978 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

SINGLE USE ACTIVE ELECTRODE HANDLE

ApplicantAspen Laboratories, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Jun 22, 1978
ReceivedJun 9, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K780978

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.