510(k) K820243 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
CONTINUOUS BLOOD PROCESSOR CBP-6000 &
| Applicant | Bentley Laboratories, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Mar 25, 1982 |
| Received | Jan 29, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K820243
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.