ClearanceBrief
510(k) K071947 ยท FMI Needle, Hypodermic, Single Lumen

VACU-MED BLOOD COLLECTION NEEDLES

ApplicantShina Corp., Minneapolis MN, US
DecisionSubstantially Equivalent, Oct 12, 2007
ReceivedJul 13, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K071947

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.