510(k) K880583 ยท MPB Catheter, Hemodialysis, Non-Implanted
MODIFIED FORMED-EXTENSION MAHURKAR DUAL LUMEN CATH
| Applicant | Quinton, Inc., Bothell WA, US |
| Decision | Substantially Equivalent, Feb 22, 1988 |
| Received | Feb 9, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880583
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.