ClearanceBrief
510(k) K942159 ยท FMF Syringe, Piston

NOVOPEN 1.5

ApplicantNovo Nordisk Pharmaceuticals, Inc., Princeton NJ, US
DecisionSubstantially Equivalent, Apr 26, 1995
ReceivedMay 3, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K942159

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.