ClearanceBrief
510(k) K951736 ยท FMI Needle, Hypodermic, Single Lumen

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ApplicantMedline, Mundelein IL, US
DecisionSubstantially Equivalent, Jul 5, 1995
ReceivedApr 13, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K951736

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.