510(k) K965178 ยท MPB Catheter, Hemodialysis, Non-Implanted
NIAGARA DUAL LUMEN CATHETER
| Applicant | Vas-Cath, Inc., Ontario, L5a 3v3, CA |
| Decision | Substantially Equivalent, Aug 19, 1997 |
| Received | Dec 24, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K965178
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.