ClearanceBrief
510(k) K853198 ยท JPA System, Multipurpose For In Vitro Coagulation Studies

ADDITIONAL HEMOTEC ACT COAGULATION CARTRIDGES

ApplicantMedical Device Consultants, Inc., North Attleboro MA, US
DecisionSubstantially Equivalent, Oct 4, 1985
ReceivedJul 30, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K853198

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.