ClearanceBrief
510(k) K043397 ยท FMI Needle, Hypodermic, Single Lumen

MODIFICATION TO BD ECLIPSE HYPODERMIC NEEDLE

ApplicantBecton, Dickinson & CO, Franklin Lakes NJ, US
DecisionSubstantially Equivalent, Dec 29, 2004
ReceivedDec 10, 2004
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K043397

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.