ClearanceBrief
510(k) K960255 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

CERAMIC BLADE ELECTRODE

ApplicantUtah Medical Products, Inc., Midvale UT, US
DecisionSubstantially Equivalent, Mar 27, 1996
ReceivedJan 17, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K960255

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.