510(k) K872652 ยท FKX System, Peritoneal, Automatic Delivery
UPGRADED AUTO PERITONEAL DIALYSIS CYCLER SYSTEM
| Applicant | Travenol Laboratories, S.A., Round Lake IL, US |
| Decision | Substantially Equivalent, Sep 30, 1987 |
| Received | Jul 7, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K872652
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.