ClearanceBrief
510(k) K901120 ยท GKP Instrument, Coagulation, Automated

KOAGULAB 60-S COAGULATION SYSTEM

ApplicantOrtho Diagnostic Systems, Inc., Raritan NJ, US
DecisionSubstantially Equivalent, May 22, 1990
ReceivedMar 12, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K901120

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.