510(k) K850406 ยท FKX System, Peritoneal, Automatic Delivery
AUTOMATIC PERITONEAL DIALYSIS CYCLER SYSTEM
| Applicant | Travenol Laboratories, S.A., Deerfield IL, US |
| Decision | Substantially Equivalent, Feb 21, 1985 |
| Received | Feb 4, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K850406
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.