ClearanceBrief
510(k) K122652 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

ARTHROCARE TURBINATOR WAND

ApplicantArthroCare Corporation, Austin TX, US
DecisionSubstantially Equivalent, Jul 2, 2013
ReceivedAug 31, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K122652

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.