510(k) K833749 ยท FKX System, Peritoneal, Automatic Delivery
PERITONEAL CATHETER-CHANGES-
| Applicant | Quinton, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Dec 27, 1983 |
| Received | Oct 26, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K833749
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.