ClearanceBrief
510(k) K802942 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

HITEMP. TM 2 LOOPTIP CAUTERY

ApplicantMedical Products Development, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Feb 4, 1981
ReceivedNov 19, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K802942

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.