510(k) K992275 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
FRESENIUS MODIFIED F400 LOW VOLUME HEMOCONCENTRATOR F3000 & MODIFIED F400 LOW VOL HEMOCONCENTRATOR W/TUBING SET F3000TS
| Applicant | Fresenius USA, Inc., Concord CA, US |
| Decision | Substantially Equivalent, Aug 4, 1999 |
| Received | Jul 7, 1999 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K992275
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.