510(k) K844108 ยท FKX System, Peritoneal, Automatic Delivery
RENAL SYSTEMS PERITONEAL ACCESS SYSTEM
| Applicant | Renal Systems, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Jan 7, 1985 |
| Received | Oct 23, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K844108
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.