510(k) K921908 ยท FMF Syringe, Piston
NOVOLINPEN DIAL-A-DOSE INSULIN DELIVERY DEVICE
| Applicant | Novo Nordisk Pharmaceuticals, Inc., Princeton NJ, US |
| Decision | Substantially Equivalent, Jun 29, 1993 |
| Received | Apr 23, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K921908
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.