510(k) K210258 ยท FMI Needle, Hypodermic, Single Lumen
NovoFine
| Applicant | Novo Nordisk, Inc., Plainsboro NJ, US |
| Decision | Substantially Equivalent, Jun 23, 2021 |
| Received | Feb 1, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K210258
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.