ClearanceBrief
510(k) K140568 ยท FMI Needle, Hypodermic, Single Lumen

CAREFINE PEN NEEDLE WITH QUINTAPOINT AND SUPERPOINT

ApplicantFacet Technologies, LLC, Kennesaw GA, US
DecisionSubstantially Equivalent, May 13, 2014
ReceivedMar 5, 2014
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K140568

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.