510(k) K844144 ยท FKX System, Peritoneal, Automatic Delivery
SCD STERILE CONNECTION DEVICE
| Applicant | E.I. Dupont DE Nemours & Co., Inc., Wilmington DE, US |
| Decision | Substantially Equivalent, Nov 16, 1984 |
| Received | Oct 23, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K844144
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.