510(k) K991623 ยท FIE Needle, Fistula
NIPRO ARTERIAL VENOUS FISTULA NEEDLE, AGULHA PARA FISTULA ARTERIO-VENOSA, AGUJA PARA FISTULA ARTERIO VENOSA
| Applicant | Nipro Medical Corp., Lexington KY, US |
| Decision | Substantially Equivalent, Aug 9, 1999 |
| Received | May 11, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K991623
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.