ClearanceBrief
510(k) K780281 ยท KSO Centrifuge, Blood-Bank For In Vitro Diagnostic Use

IMMUFUGE DISP. LINER

ApplicantDade, Baxter Travenol Diagnostics, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Mar 2, 1978
ReceivedFeb 21, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K780281

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.