ClearanceBrief
510(k) K821898 ยท DBA Complement C1 Inhibitor (Inactivator), Antigen, Antiserum, Control

ORTHO CLASSICAL PATHWAY COMPL. TEST

ApplicantOrtho Diagnostic Systems, Inc., Carpinteria CA, US
DecisionSubstantially Equivalent, Jul 16, 1982
ReceivedJun 28, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K821898

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.