ClearanceBrief
510(k) K082666 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

ARTHROCARE CONTROLLER (SYSTEM 12000), ARTHROCARE PATIENT CABLE, FOOT CONTROL, POWER CORD, WANDS

ApplicantArthrocare Corp., Sunnyvale CA, US
DecisionSubstantially Equivalent, Oct 15, 2008
ReceivedSep 12, 2008
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K082666

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.