510(k) K182387 ยท FMF Syringe, Piston
NovoPen Echo Dial-A-Dose Insulin Delivery Device (Pen Injector)
| Applicant | Novo Nordisk, Inc., Plainsboro NJ, US |
| Decision | Substantially Equivalent, Dec 17, 2018 |
| Received | Sep 4, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K182387
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.