Fresenius 2008K
FDA 510(k) K994267 · Fresenius Medical Care
510(k) numberK994267
Submission
- Device name
- Fresenius 2008K
- Applicant
- Fresenius Medical Care
Lexington, MA, US - Received
- December 17, 1999
- Decision date
- March 16, 2000
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- KDI – Dialyzer, High Permeability With Or Without Sealed Dialysate System
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 876.5860
- Specialty
- Gastroenterology, Urology
- Life-sustaining
- Yes
Other 510(k)s with product code KDI
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K261267 | Careflux H60;Careflux H70;Careflux V500KDI · Traditional | Fresenius Medical Care Renal Therapies Group, LLC | 07/24/2026SE |
| K252377 | NxStage System One with NxViewKDI · Traditional | Fresenius Medical Care Renal Therapies Group, LLC | 05/15/2026SE |
| K260533 | Elisio-HKDI · Special | Nipro Medical Corporation | 03/19/2026SE |
| K252459 | multiFlux 130 (F00013123); multiFlux 160 (F00013124)KDI · Traditional | Fresenius Medical Care Renal Therapies Group, LLC | 02/10/2026SE |
| K253412 | Tablo Hemodialysis System (PN-0008000, PN-0006000U)KDI · Traditional | Outset Medical, Inc. | 01/26/2026SE |
| K253518 | FX CorAL 40; FX CorAL 50KDI · Special | Fresenius Medical Care Renal Therapies Group, LLC | 12/18/2025SE |
| K243920 | Purema H Hemoconcentrator - PediatricKDI · Traditional | Medica USA, Inc. | 09/19/2025SE |
| K250508 | AK 98 Dialysis Machine (955607)KDI · Traditional | Vantive US Healthcare, LLC | 08/01/2025SE |
| K243237 | 2008T HD SYS. CDX BLUESTAR (191124); 2008T HD SYS. CDX W/bibag BLUESTAR (191126); 2008T…KDI · Traditional | Fresenius Medical Care Renal Therapies Group, LLC | 06/13/2025SE |
| K243505 | 5008X Hemodialysis SystemKDI · Traditional | Fresenius Medical Care Renal Therapies Group, LLC | 05/30/2025SE |
More from Fresenius Medical Care Renal Therapies Group, LLC
| 510(k) | Device | Decision |
|---|---|---|
| K231534 | 5008X Hemodialysis SystemKDI · Traditional | 02/02/2024SE |
| K141997 | Crit-Line IV SystemKOC · Traditional | 04/01/2015SE |
| K111639 | Fresenius 2008T Hemodialysis MachineKDI · Special | 10/21/2011SE |
| K030497 | Fresenius Naturalyte Granuflo Dry Acid Concentrate 10XX Series, 24XX Series, 30XX SeriesKPO · Traditional | 05/20/2003SE |
| K023162 | Fresenius Punctur-Guard Fistula Needle SetsFIE · Traditional | 03/20/2003SE |
| K022536 | \Resenius Access Flow Reserving Connectors, Fresenius Standalone Accces Flow Reserving…KOC · Traditional | 10/30/2002SE |
Questions and answers
When was Fresenius 2008K cleared by the FDA?
Fresenius 2008K (K994267) received a 510(k) decision of Substantially Equivalent on March 16, 2000, 90 days after the submission was received.
What is the product code of K994267?
The FDA product code is KDI – Dialyzer, High Permeability With Or Without Sealed Dialysate System, a Class II (moderate risk) device regulated under 21 CFR 876.5860.