ClearanceBrief
510(k) K924793 ยท FMI Needle, Hypodermic, Single Lumen

HAN-D-AID

ApplicantSalmon Ent., Hudson IL, US
DecisionSubstantially Equivalent, Oct 19, 1993
ReceivedSep 23, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K924793

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.