510(k) K830766 ยท FKX System, Peritoneal, Automatic Delivery
ABBOTT PATIENT ASSIST DEVICE
| Applicant | Abbott Laboratories, Abbott Park IL, US |
| Decision | Substantially Equivalent, Mar 29, 1983 |
| Received | Mar 10, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K830766
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.