ClearanceBrief
510(k) K012526 ยท FPA Set, Administration, Intravascular

BIOTEQUE SCALP VEIN SET

ApplicantBioteque Corp., Flaggstaff AZ, US
DecisionSubstantially Equivalent, Sep 14, 2001
ReceivedAug 6, 2001
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K012526

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.