ClearanceBrief
510(k) K143235 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

RF20000a Controller, FLOW 50 Wand

ApplicantArthroCare Corporation, Austin TX, US
DecisionSubstantially Equivalent, Oct 23, 2015
ReceivedNov 10, 2014
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K143235

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.