510(k) K071518 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
DIACAP LO PS (10, 12, 15) AND DIACAP HI PS (10, 12, 15, 18, 20) HEMODIALYZERS
| Applicant | B. Braun Medizintechnologie GmbH, Melsungen, DE |
| Decision | Substantially Equivalent, Aug 17, 2007 |
| Received | Jun 4, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K071518
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.