510(k) K903641 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
QUICK PRIME HEMOCONCEN. NO. HQ-7000 AND CBP-7000Q
| Applicant | Bentley Laboratories, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Nov 9, 1990 |
| Received | Aug 14, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K903641
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.