ClearanceBrief
510(k) K833636 ยท DAK Complement C1q, Antigen, Antiserum, Control

ORTHO* SERUM ELISA TEST SYSTEM

ApplicantOrtho Diagnostic Systems, Inc., Carpinteria CA, US
DecisionSubstantially Equivalent, Jun 13, 1984
ReceivedOct 17, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K833636

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.