ClearanceBrief
510(k) K992699 ยท FMI Needle, Hypodermic, Single Lumen

NIPRO BLOOD COLLECTION NEEDLE

ApplicantNipro Medical Corp., Lexington KY, US
DecisionSubstantially Equivalent, Feb 14, 2000
ReceivedAug 12, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K992699

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.