510(k) K822025 ยท FKX System, Peritoneal, Automatic Delivery
AUTOMATIC SPLICING DEVICE
| Applicant | E.I. Dupont DE Nemours & Co., Inc., Walker MI, US |
| Decision | Substantially Equivalent, Sep 9, 1982 |
| Received | Jul 12, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K822025
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.