ClearanceBrief
510(k) K904073 ยท GGC Control, Plasma, Abnormal

COAGULATION REFERENCE PLASMA, ABNORMAL

ApplicantMedi-Tech, Inc., Ventura CA, US
DecisionSubstantially Equivalent, Oct 22, 1990
ReceivedSep 5, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K904073

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.