510(k) K992894 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
MERIDIAN HEMODIALYSIS MACHINE, MODEL 5M5576
| Applicant | Baxter Healthcare Corp, Mcgaw Park IL, US |
| Decision | Substantially Equivalent, Nov 24, 1999 |
| Received | Aug 27, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K992894
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Nov 14, 2006 | Baxter Healthcare Renal Div Meridian Hemodialysis Instrument, product code 5M5576 and 5M5576R; Baxter Healthcare Corporation, Renal Division, McGaw Park, IL 60085 U.S.A. Terminated |
KDI | None listed |
| Dec 14, 2005 | Baxter Healthcare Renal Div Baxter Meridian Hemodialysis Instrument, product codes 5M5576 and 5M5576R; Baxter Healthcare Corporation, Renal Division, McGaw Park, IL 60085 U.S.A. Terminated |
KDI | None listed |
| Jun 30, 2005 | Baxter Healthcare Renal Div Baxter Meridian Hemodialysis Instrument, product codes 5M5576 and 5M5576R; Baxter Healthcare Corporation, Renal Division, McGaw Park, IL 60085 U.S.A. Terminated |
KDI | None listed |
| Dec 8, 2004 | Baxter Healthcare Renal Div Baxter Meridian Hemodialysis Instrument, product codes 5M5576 and 5M5576R; Baxter Healthcare Corporation, Renal Division, McGaw Park, IL 60085 U.S.A. Terminated |
KDI | None listed |
| Jul 20, 2004 | Baxter Healthcare Renal Div Baxter Meridian Hemodialysis Instrument, product codes 5M5576 and 5M5576R; Baxter Healthcare Corporation, Renal Division, McGaw Park, IL 60085 U.S.A. Terminated |
KDI | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.