510(k) K935659 ยท FKX System, Peritoneal, Automatic Delivery
BAXTER NIGHT EXCH DEVICE(NXD) PERITONEAL DIALY SYST
| Applicant | Baxter Healthcare Corp, Mcgaw Park IL, US |
| Decision | Substantially Equivalent, Jul 7, 1994 |
| Received | Nov 24, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K935659
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.