510(k) K964514 ยท FKO Catheter, Peritoneal Dialysis, Single Use
CORPAK MEDSYSTEMS CRUZ CATHETER FOR PERITONEAL DIALYSIS
| Applicant | Corpak, Inc., Wheeling IL, US |
| Decision | Substantially Equivalent, Jun 26, 1998 |
| Received | Oct 29, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K964514
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.