510(k) K896252 ยท MPB Catheter, Hemodialysis, Non-Implanted
MODIFIED QUINTON SINGLE LUMEN CATHETER
| Applicant | Quinton, Inc., Bothell WA, US |
| Decision | Substantially Equivalent, Jan 29, 1990 |
| Received | Oct 30, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896252
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.