510(k) K955002 ยท MPB Catheter, Hemodialysis, Non-Implanted
MAHURKAR 8 FR DUAL LEMEN CATHETER
| Applicant | Quinton, Inc., Bothell WA, US |
| Decision | Substantially Equivalent, Sep 13, 1996 |
| Received | Nov 1, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K955002
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.