ClearanceBrief
510(k) K944230 ยท FMI Needle, Hypodermic, Single Lumen

DIAL MEDICAL SUPPLY SHARPS CONTAINER

ApplicantRegulatory & Marketing Services, Inc., Palm Harbor FL, US
DecisionSubstantially Equivalent, Nov 7, 1994
ReceivedAug 31, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K944230

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.