ClearanceBrief
510(k) K210749 ยท KPE Container, I.V.

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ApplicantHaemotronic S.P.A., Mirandola, IT
DecisionSubstantially Equivalent, Aug 19, 2021
ReceivedMar 12, 2021
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K210749

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.