ClearanceBrief
510(k) K220563 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

Ambient HipVac 50 Wand with Integrated Finger Switches, RF20000 COBLATION System, WEREWOLF COBLATION System, WEREWOLF+ COBLATION System

ApplicantArthroCare Corporation, Austin TX, US
DecisionSubstantially Equivalent, Sep 1, 2022
ReceivedFeb 28, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K220563

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.