510(k) K830257 ยท FKX System, Peritoneal, Automatic Delivery
NON-STERILE PERITONEAL ACCESS CATHET-
| Applicant | Evermed, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 24, 1983 |
| Received | Jan 25, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K830257
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.