ClearanceBrief
510(k) K896918 ยท DEH Lambda, Antigen, Antiserum, Control

MOUSE ANTI-HUMAN LEUCOCYTE ANTIGEN & DAKO PAP KIT

ApplicantDako Corp., Carpinteria CA, US
DecisionSubstantially Equivalent, Aug 27, 1990
ReceivedDec 11, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K896918

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.