ClearanceBrief
510(k) K123353 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

CIQ CONTROLLER, CIQ WANDS

ApplicantArthroCare Corporation, Austin TX, US
DecisionSubstantially Equivalent, Apr 5, 2013
ReceivedOct 31, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K123353

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.