510(k) K992653 ยท FIE Needle, Fistula
SHELLY PROTECTED AV FISTULA NEEDLE
| Applicant | Diasol, Inc., North Hollywood CA, US |
| Decision | Substantially Equivalent, Oct 27, 1999 |
| Received | Aug 6, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K992653
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.