510(k) K062953 ยท FIE Needle, Fistula
MEDISYSTEMS ARTERIAL-VENOUS FISTULA NEEDLE SET WITH SECUREMENT DEVICE
| Applicant | Medisystems Corp., Seattle WA, US |
| Decision | Substantially Equivalent, Feb 12, 2007 |
| Received | Sep 29, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K062953
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.