ClearanceBrief
510(k) K093008 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories

HALO ABLATION CATHETER, MODEL 90-9100

ApplicantBarrx Medical, Incorporated, Sunnyvale CA, US
DecisionSubstantially Equivalent, Jan 8, 2010
ReceivedSep 28, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K093008

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.