ClearanceBrief
510(k) K170988 ยท FMI Needle, Hypodermic, Single Lumen

DropSafe Safety Pen Needle

ApplicantHtl-Strefa S.A, Ozorkow, PL
DecisionSubstantially Equivalent, Dec 12, 2017
ReceivedApr 3, 2017
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K170988

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.