510(k) K963446 ยท MPB Catheter, Hemodialysis, Non-Implanted
KENDALL DUAL LUMEN CATHETER
| Applicant | Kendall Healthcare Products Co. Div.Of Tyco Health, Mansfield MA, US |
| Decision | Substantially Equivalent, Mar 18, 1997 |
| Received | Sep 3, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K963446
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.