510(k) K963658 ยท FMI Needle, Hypodermic, Single Lumen
EXEL AVF SINGLE NEEDLE
| Applicant | Exel Intl., Culver City CA, US |
| Decision | Substantially Equivalent, May 5, 1998 |
| Received | Sep 3, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K963658
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.