510(k) K971180 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
BARD NO-RINSE HEMOCONCENTRATOR AND ACCESSORY KIT
| Applicant | C.R. Bard, Inc., Haverhill MA, US |
| Decision | Substantially Equivalent, Jul 24, 1997 |
| Received | Mar 31, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K971180
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.