ClearanceBrief
510(k) K231151 ยท DGC Ige, Antigen, Antiserum, Control

Kenota 1 Total IgE; Kenota 1 (instrument)

ApplicantKenota, Inc., Kitchener, CA
DecisionSubstantially Equivalent, May 31, 2024
ReceivedApr 24, 2023
TypeDual Track
FDA recordOpen on fda.gov

Recalls that name K231151

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.