510(k) K231255 · FMI Needle, Hypodermic, Single Lumen
NovoFine® Plus
| Applicant | Novo Nordisk, Inc., Plainsboro NJ, US |
| Decision | Substantially Equivalent, Aug 25, 2023 |
| Received | May 1, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K231255
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.