ClearanceBrief
510(k) K854376 ยท JPA System, Multipurpose For In Vitro Coagulation Studies

HEMOTEC CITRATED WHOLE BLOOD COAGULATION CONTROLS

ApplicantHemotec, Inc., Attleboro MA, US
DecisionSubstantially Equivalent, Dec 4, 1985
ReceivedOct 30, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K854376

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.