510(k) K822361 ยท FKX System, Peritoneal, Automatic Delivery
DIANEAL SOLUTION EXCHANGE DEVICE #5C4193
| Applicant | Travenol Laboratories, S.A., Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 16, 1982 |
| Received | Aug 6, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K822361
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.