ClearanceBrief
510(k) K093109 ยท FMI Needle, Hypodermic, Single Lumen

NOVOTWIST NEEDLE, MODELS 30G * 8MM (1/3) 32 G TIP * 5 MM(1/5')

ApplicantNovo Nordisk, Inc., Princeton NJ, US
DecisionSubstantially Equivalent, Jun 18, 2010
ReceivedOct 1, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K093109

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.