ClearanceBrief
510(k) K954500 ยท FMI Needle, Hypodermic, Single Lumen

HOSPITEC MEDI-BUTLER

ApplicantHospitec, Inc., Saint Paul MN, US
DecisionSubstantially Equivalent, Jan 18, 1996
ReceivedSep 28, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K954500

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.