ClearanceBrief
510(k) K173479 ยท FMI Needle, Hypodermic, Single Lumen

NovoFine 32G Tip (0.23/0.25) x 6 mm ETW (extra thin wall)

ApplicantNovo Nordisk, Inc., Plainsboro NJ, US
DecisionSubstantially Equivalent, Jan 17, 2018
ReceivedNov 13, 2017
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K173479

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.