510(k) K905793 ยท FKP System, Dialysate Delivery, Single Patient
COBE CENTRY 2 BICART OPTION KIT
| Applicant | Cobe Laboratories, Inc., Lakewood CO, US |
| Decision | Substantially Equivalent, Feb 12, 1991 |
| Received | Dec 27, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K905793
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.