510(k) K760544 ยท FKO Catheter, Peritoneal Dialysis, Single Use
CATHETER, PERITONEAL DIALYSIS
| Applicant | Travenol Laboratories, S.A., Mchenry IL, US |
| Decision | Substantially Equivalent, Oct 20, 1976 |
| Received | Aug 30, 1976 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K760544
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.