ClearanceBrief
510(k) K041890 ยท OCL Surgical Device, For Cutting, Coagulation, And/Or Ablation Of Tissue, Including Cardiac Tissue

CRYOCOR MODEL 1250 (BREVA) SERIES SURGICAL PROBES, MODEL 1255-15-12

ApplicantCryocor, Inc., San Diego CA, US
DecisionSubstantially Equivalent, Sep 22, 2004
ReceivedJul 12, 2004
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K041890

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.