ClearanceBrief
510(k) K884590 ยท KFF Assay, Heparin

HEPCON/SYSTEM B-10 HEPARIN ASSAY/SCREEN/CARTRIDGES

ApplicantHemotec, Inc., Englewood CO, US
DecisionSubstantially Equivalent, Jan 10, 1989
ReceivedNov 3, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K884590

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.