ClearanceBrief
510(k) K791462 ยท FMI Needle, Hypodermic, Single Lumen

HYPERDERMIC NEEDLE WITH SENSOR #514

ApplicantMedtech Intl., Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Sep 24, 1979
ReceivedJul 16, 1979
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K791462

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.