510(k) K811986 ยท FKX System, Peritoneal, Automatic Delivery
THE AMP 80/2 PEDIATRIC CYCLER SYSTEM
| Applicant | American Medical Products, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 31, 1981 |
| Received | Jul 13, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K811986
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.