ClearanceBrief
510(k) K151133 ยท GKZ Counter, Differential Cell

PENTRA XLR

ApplicantHORIBA ABX SAS, Montpellier, FR
DecisionSubstantially Equivalent, Dec 9, 2015
ReceivedApr 28, 2015
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K151133

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.