ClearanceBrief
510(k) K940331 ยท DEH Lambda, Antigen, Antiserum, Control

KERATIN PRIMARY ANTIBODY

ApplicantVentana Medical Systems, Inc., Tucson AZ, US
DecisionSubstantially Equivalent, Feb 26, 1996
ReceivedJan 24, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K940331

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.