ClearanceBrief
510(k) K883688 ยท GJT Plasma, Coagulation Factor Deficient

ORTHO FACTOR XII DEFICIENT PLASMA

ApplicantOrtho Diagnostic Systems, Inc., Raritan NJ, US
DecisionSubstantially Equivalent, Nov 1, 1988
ReceivedAug 29, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K883688

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.