510(k) K823857 ยท FKX System, Peritoneal, Automatic Delivery
IMPRA PERITONEAL CATHETER
| Applicant | Impra, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Jan 26, 1983 |
| Received | Dec 22, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K823857
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.