ClearanceBrief
510(k) K912800 ยท DGC Ige, Antigen, Antiserum, Control

KALLESTEAD TOTAL IGE MICROPLATE KIT

ApplicantBio-Rad Laboratories, Inc., Chaska MN, US
DecisionSubstantially Equivalent, Jul 25, 1991
ReceivedJun 25, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K912800

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.