ClearanceBrief
510(k) K951968 ยท DAK Complement C1q, Antigen, Antiserum, Control

HUMAN C1Q RADIAL IMMUNODIFFUSION KIT

ApplicantKent Laboratories, Inc., Redmond WA, US
DecisionSubstantially Equivalent, May 30, 1995
ReceivedApr 27, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K951968

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.