ClearanceBrief
510(k) K971924 ยท FMI Needle, Hypodermic, Single Lumen

BLUNT SYRINGE CANNULA

ApplicantB.Braun Medical, Inc., Bethlehem PA, US
DecisionSubstantially Equivalent, Sep 25, 1998
ReceivedMay 23, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K971924

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.