510(k) K823777 ยท FKX System, Peritoneal, Automatic Delivery
STERILE, DISPOS. SPIKE PROTECTOR-5C4138
| Applicant | Travenol Laboratories, S.A., Walker MI, US |
| Decision | Substantially Equivalent, Jan 7, 1983 |
| Received | Dec 15, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K823777
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.