ClearanceBrief
510(k) K812637 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

ACMI BIPOLAR HEMOSTATIC SOURCE

ApplicantAmerican Cystocope Makers, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Oct 26, 1981
ReceivedSep 15, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K812637

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.