510(k) K982399 ยท FMI Needle, Hypodermic, Single Lumen
DISETRONIC PENFINE INJECTION PEN NEEDLE
| Applicant | Disetronic Medical Systems, Fort Myers FL, US |
| Decision | Substantially Equivalent, Aug 6, 1998 |
| Received | Jul 10, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K982399
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.