510(k) K013782 ยท FMI Needle, Hypodermic, Single Lumen
DISETRONIC PENFINE INSULIN INJECTION PEN NEEDLE
| Applicant | Disetronic Medical Systems, St. Paul MN, US |
| Decision | Substantially Equivalent, Nov 20, 2001 |
| Received | Nov 14, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013782
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.