510(k) K002403 ยท FMI Needle, Hypodermic, Single Lumen
NOVOFINE 31 DISPOSABLE NEEDLE
| Applicant | Novo Norodisk Pharmaceuticals, Inc., Princeton NJ, US |
| Decision | Substantially Equivalent, Dec 8, 2000 |
| Received | Aug 7, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K002403
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.