510(k) K062500 ยท FMI Needle, Hypodermic, Single Lumen
FLEXPEN NEEDLE
| Applicant | Novo Nordisk, Inc., Princeton NJ, US |
| Decision | Substantially Equivalent, Nov 21, 2006 |
| Received | Aug 25, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K062500
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.