ClearanceBrief
510(k) K083737 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

HALO ABLATION CATHETER

ApplicantBarrx Medical, Incorporated, Sunnyvale CA, US
DecisionSubstantially Equivalent, Feb 10, 2009
ReceivedDec 16, 2008
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K083737

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.