ClearanceBrief
510(k) K150251 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

Barrx Anorectal RFA Wand

ApplicantCovidien, LLC, Mansfield MA, US
DecisionSubstantially Equivalent, Jul 28, 2015
ReceivedFeb 3, 2015
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K150251

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.