ClearanceBrief
510(k) K002449 ยท FPA Set, Administration, Intravascular

BIOTEQ I.V. (INTRAVENOUS) SET

ApplicantBioteque Corp., Flaggstaff AZ, US
DecisionSubstantially Equivalent, Dec 22, 2000
ReceivedAug 9, 2000
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K002449

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.