510(k) K830208 ยท FKX System, Peritoneal, Automatic Delivery
BETA-CAP D ADAPTER
| Applicant | Quinton, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Mar 7, 1983 |
| Received | Jan 21, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K830208
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.