ClearanceBrief
510(k) K942073 ยท FMI Needle, Hypodermic, Single Lumen

SHARPSPRO-TECTOR

ApplicantSuperior Diapering Products , Ltd., Point Roberts WA, US
DecisionSubstantially Equivalent, Feb 29, 1996
ReceivedApr 29, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K942073

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.