ClearanceBrief
510(k) K221493 ยท LIE Reagent/Device, Inoculum Calibration

MicroScan Prompt Inoculation System-D

ApplicantBeckman Coulter, Inc., West Sacramento CA, US
DecisionSubstantially Equivalent, Apr 5, 2023
ReceivedMay 23, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K221493

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.