510(k) K823092 ยท FKQ System, Dialysate Delivery, Central Multiple Patient
HEMAFLO BLOOD TUBING SETS
| Applicant | Cobe Laboratories, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Nov 22, 1982 |
| Received | Oct 20, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K823092
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.