510(k) K955182 ยท FIE Needle, Fistula
NIPRO ARTERIAL VENOUS FISTULA NEEDLE
| Applicant | Nissho Corp., Miami FL, US |
| Decision | Substantially Equivalent, Jun 4, 1996 |
| Received | Nov 13, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K955182
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.