Bicarby Dialysate RFP-402 (RFP-402-G); Bicarby Dialysate RFP-400 (RFP-400-G); Bicarby Dialysate RFP-407 (RFP-407-G); Bicarby Dialysate RFP-401 (RFP-401-G); Bicarby Dialysate RFP-404 (RFP-404-G); Bicarby Dialysate RFP-456 (RFP-456-G); Ci-Ca Dialysate 2K (RFP-457-G); Ci-Ca Dialysate 4K (RFP-458-G)

FDA 510(k) K243786 · Fresenius Medical Care Renal Therapies Group, LLC

Substantially Equivalent

510(k) numberK243786

Submission

Device name
Bicarby Dialysate RFP-402 (RFP-402-G); Bicarby Dialysate RFP-400 (RFP-400-G); Bicarby Dialysate RFP-407 (RFP-407-G); Bicarby Dialysate RFP-401 (RFP-401-G); Bicarby Dialysate RFP-404 (RFP-404-G); Bicarby Dialysate RFP-456 (RFP-456-G); Ci-Ca Dialysate 2K (RFP-457-G); Ci-Ca Dialysate 4K (RFP-458-G)
Applicant
Fresenius Medical Care Renal Therapies Group, LLC
Waltham, MA, US
Received
December 9, 2024
Decision date
April 4, 2025
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
KPO – Dialysate Concentrate For Hemodialysis (Liquid Or Powder)
Device class
Class II (moderate risk)
Regulation
21 CFR 876.5820
Specialty
Gastroenterology, Urology
Life-sustaining
Yes

Other 510(k)s with product code KPO

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K260799Nipro Dry Acid Concentrate MixerKPO · Traditional Nipro Technical Solutions, Incoporated08/19/2026SE
K253462NaturaLyte® Dry Bicarbonate Concentrate (08-4112-2)KPO · Traditional Fresenius Medical Care Renal Therapies Group, LLC01/29/2026SE
K252180Bicarby Dialysate RFP-404 (RFP-404-W); Bicarby Dialysate RFP-403 (RFP-403-W); Bicarby…KPO · Traditional Fresenius Medical Care Renal Therapies Group, LLC09/09/2025SE
K240920HemoCare Bicarbonate Concentrate Set (BCS)KPO · Traditional Deka Research and Development07/12/2024SE
K233950pureFLOW 402 (F00012067); pureFLOW 406 (F00012068); pureFLOW 401 (F00012069); pureFLOW…KPO · Traditional Fresenius Medical Care Renal Therapies Group, LLC05/10/2024SE
K233213NxStage PureFlow SolutionKPO · Traditional Nxstage Medical, Inc.01/18/2024SE
K233159pureFLOW 402, pureFLOW 400, pureFLOW 406, pureFLOW 401, pureFLOW 502, pureFLOW 504KPO · Traditional Fresenius Medical Care Renal Therapies Group, LLC12/01/2023SE
K223431Citric Complete Liquid Citric Acid ConcentrateKPO · Traditional Nipro Renal Solutions USA, Corp.08/04/2023SE
K221652NikkicartKPO · Traditional Renal Care Dialysis Solutions, S.A. DE C.V.03/03/2023SE
K202508Hemo-Lyte C CartridgeKPO · Traditional Di-Chem, Inc.08/12/2022SE

More from Di-Chem, Inc.

510(k)DeviceDecision
K261267Careflux H60;Careflux H70;Careflux V500KDI · Traditional 07/24/2026SE
K252377NxStage System One with NxViewKDI · Traditional 05/15/2026SE
K252459multiFlux 130 (F00013123); multiFlux 160 (F00013124)KDI · Traditional 02/10/2026SE
K253462NaturaLyte® Dry Bicarbonate Concentrate (08-4112-2)KPO · Traditional 01/29/2026SE
K253518FX CorAL 40; FX CorAL 50KDI · Special 12/18/2025SE
K250634BCM2-Body Composition MonitorDSB · Traditional 11/24/2025SE
K250471AquaC UNO HFIP · Traditional 11/14/2025SE
K251851DIASAFEplusUS (F00013010)FIP · Traditional 10/09/2025SE
K252180Bicarby Dialysate RFP-404 (RFP-404-W); Bicarby Dialysate RFP-403 (RFP-403-W); Bicarby…KPO · Traditional 09/09/2025SE
K2432372008T HD SYS. CDX BLUESTAR (191124); 2008T HD SYS. CDX W/bibag BLUESTAR (191126); 2008T…KDI · Traditional 06/13/2025SE

Questions and answers

When was Bicarby Dialysate RFP-402 (RFP-402-G); Bicarby Dialysate RFP-400 (RFP-400-G); Bicarby Dialysate RFP-407 (RFP-407-G); Bicarby Dialysate RFP-401 (RFP-401-G); Bicarby Dialysate RFP-404 (RFP-404-G); Bicarby Dialysate RFP-456 (RFP-456-G); Ci-Ca Dialysate 2K (RFP-457-G); Ci-Ca Dialysate 4K (RFP-458-G) cleared by the FDA?

Bicarby Dialysate RFP-402 (RFP-402-G); Bicarby Dialysate RFP-400 (RFP-400-G); Bicarby Dialysate RFP-407 (RFP-407-G); Bicarby Dialysate RFP-401 (RFP-401-G); Bicarby Dialysate RFP-404 (RFP-404-G); Bicarby Dialysate RFP-456 (RFP-456-G); Ci-Ca Dialysate 2K (RFP-457-G); Ci-Ca Dialysate 4K (RFP-458-G) (K243786) received a 510(k) decision of Substantially Equivalent on April 4, 2025, 116 days after the submission was received.

What is the product code of K243786?

The FDA product code is KPO – Dialysate Concentrate For Hemodialysis (Liquid Or Powder), a Class II (moderate risk) device regulated under 21 CFR 876.5820.