ClearanceBrief
510(k) K061933 ยท FMI Needle, Hypodermic, Single Lumen

HAGER MIRAMATIC BOX SHARPS CONTAINER AND CAP TRAP NEEDLE RE-CAPPER

ApplicantHager Worldwide, Inc., Andover MA, US
DecisionSubstantially Equivalent, Nov 16, 2006
ReceivedJul 7, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K061933

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.