510(k) K010359 ยท FMF Syringe, Piston
INNOVO
| Applicant | Novo Nordisk A/S, Princeton NJ, US |
| Decision | Substantially Equivalent, Mar 14, 2001 |
| Received | Feb 6, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K010359
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.