ClearanceBrief
510(k) K864541 ยท FMF Syringe, Piston

BT HYPODERMIC SYRINGE

ApplicantBaron Technologies, Inc., Salt Lake City UT, US
DecisionSubstantially Equivalent, Jan 21, 1987
ReceivedNov 19, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K864541

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.