510(k) K001496 ยท FIE Needle, Fistula
A.V. FISTULA NEEDLE
| Applicant | Exelint International, Co., Los Angeles CA, US |
| Decision | Substantially Equivalent, Aug 1, 2000 |
| Received | May 15, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K001496
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.