Citric Complete Liquid Citric Acid Concentrate

FDA 510(k) K223431 · Nipro Renal Solutions USA, Corp.

Substantially Equivalent

510(k) numberK223431

Submission

Device name
Citric Complete Liquid Citric Acid Concentrate
Applicant
Nipro Renal Solutions USA, Corp.
Lewisberry, PA, US
Received
November 14, 2022
Decision date
August 4, 2023
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
K243786Bicarby Dialysate RFP-402 (RFP-402-G); Bicarby Dialysate RFP-400 (RFP-400-G); Bicarby…KPO · Traditional Fresenius Medical Care Renal Therapies Group, LLC04/04/2025SE
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
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
K193155Nipro Dry Complete Dry Acid Concentrate for HemodialysisKPO · Traditional 11/25/2020SE

Questions and answers

When was Citric Complete Liquid Citric Acid Concentrate cleared by the FDA?

Citric Complete Liquid Citric Acid Concentrate (K223431) received a 510(k) decision of Substantially Equivalent on August 4, 2023, 263 days after the submission was received.

What is the product code of K223431?

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.