510(k) K874632 ยท FKX System, Peritoneal, Automatic Delivery
BENT NECK CURLCATH PERITONEAL DIALYSIS KIT
| Applicant | Quinton, Inc., Seattle WA, US |
| Decision | Substantially Equivalent, Dec 29, 1987 |
| Received | Nov 9, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K874632
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.