ClearanceBrief
510(k) K942624 ยท FMI Needle, Hypodermic, Single Lumen

LOK-ON NEEDLE DISPOSAL CONTAINER

ApplicantMedical Safety Products, Inc., Englewood CO, US
DecisionSubstantially Equivalent, Aug 25, 1994
ReceivedJun 1, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K942624

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.