ClearanceBrief
510(k) K003521 ยท FMI Needle, Hypodermic, Single Lumen

DISPO-MED 7.6 LITER SHARPS CONTAINER

ApplicantMaster Benefits, Inc., Hayward CA, US
DecisionSubstantially Equivalent, Apr 19, 2001
ReceivedNov 14, 2000
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K003521

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.