ClearanceBrief
510(k) K823923 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

MF 360B ELECTROSURGICAL UNIT

ApplicantAspen Laboratories, Inc., Walker MI, US
DecisionSubstantially Equivalent, Feb 15, 1983
ReceivedDec 28, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K823923

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.