ClearanceBrief
510(k) K940645 ยท FMI Needle, Hypodermic, Single Lumen

KEY-LOK(TM) SYSTEM

ApplicantSt. Paul Medical, Coon Rapids MN, US
DecisionSubstantially Equivalent, Nov 20, 1995
ReceivedFeb 15, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K940645

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.