510(k) K823827 ยท FKX System, Peritoneal, Automatic Delivery
AMP 80/2 OUTFLOW MONITOR MODIFICATION
| Applicant | American Medical Products, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Mar 17, 1983 |
| Received | Dec 20, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K823827
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.