ClearanceBrief
510(k) K113265 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

GENII GI 4000 ELECTROSUGICAL GENERATOR

ApplicantGenii, Inc., Austin TX, US
DecisionSubstantially Equivalent, Mar 22, 2012
ReceivedNov 4, 2011
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K113265

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.