ClearanceBrief
510(k) K933274 ยท FMI Needle, Hypodermic, Single Lumen

ONGARD 3 QUART SHARPS CONTAINER

ApplicantOngard Systems, Inc., Denver CO, US
DecisionSubstantially Equivalent, May 16, 1994
ReceivedJul 6, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K933274

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.