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FDA 510(k)

Citrasate Liquid Acid Concentrate, NaturaLyte Liquid Acid Concentrate

K-Number: K212620 · 2022-05-12

ApplicantFresenius Medical Care Renal Therapies Group, LLC
Decision Date2022-05-12
Product CodeKPO
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Citrasate Liquid Acid Concentrate, NaturaLyte Liquid Acid Concentrate is the device name listed in this FDA 510(k) record. The listed applicant is Fresenius Medical Care Renal Therapies Group, LLC. It received FDA 510(k) clearance on 2022-05-12 under 510(k) number K212620. The device is classified under product code KPO. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Citrasate Liquid Acid Concentrate, NaturaLyte Liquid Acid Concentrate?

Citrasate Liquid Acid Concentrate, NaturaLyte Liquid Acid Concentrate is a medical device that received FDA 510(k) clearance on 2022-05-12. The listed applicant is Fresenius Medical Care Renal Therapies Group, LLC. The 510(k) number is K212620.

When did Citrasate Liquid Acid Concentrate, NaturaLyte Liquid Acid Concentrate receive FDA 510(k) clearance?

Citrasate Liquid Acid Concentrate, NaturaLyte Liquid Acid Concentrate received FDA 510(k) clearance on 2022-05-12, under 510(k) number K212620.

Who is the listed applicant for Citrasate Liquid Acid Concentrate, NaturaLyte Liquid Acid Concentrate?

The FDA 510(k) record lists Fresenius Medical Care Renal Therapies Group, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Citrasate Liquid Acid Concentrate, NaturaLyte Liquid Acid Concentrate?

The FDA product code for Citrasate Liquid Acid Concentrate, NaturaLyte Liquid Acid Concentrate is KPO.

Other records listing Fresenius Medical Care Renal Therapies Group, LLC as applicant

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K261267Careflux H60;Careflux H70;Careflux V500K252377NxStage System One with NxViewK252459multiFlux 130 (F00013123); multiFlux 160 (F00013124)K253462NaturaLyte® Dry Bicarbonate Concentrate (08-4112-2)K253518FX CorAL 40; FX CorAL 50K250634BCM2-Body Composition Monitor

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Related Devices (Code: KPO)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K253462NaturaLyte® Dry Bicarbonate Concentrate (08-4112-2)Fresenius Medical Care Renal Therapies Group, LLCK252180Bicarby Dialysate RFP-404 (RFP-404-W); Bicarby Dialysate RFP-403 (RFP-403-W); Bicarby Dialysate RFP-403 (RFP-403-G); Bicarby Dialysate RFP-453 (RFP-453-W); Bicarby Dialysate RFP-453 (RFP-453-G); Bicarby Dialysate RFP-454 (RFP-454-W); Bicarby Dialysate RFP-454 (RFP-454-G); Bicarby Dialysate RFP-456 (RFP-456-W)Fresenius Medical Care Renal Therapies Group, LLCK243786Bicarby 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)Fresenius Medical Care Renal Therapies Group, LLCK240920HemoCare Bicarbonate Concentrate Set (BCS)Deka Research and DevelopmentK233950pureFLOW 402 (F00012067); pureFLOW 406 (F00012068); pureFLOW 401 (F00012069); pureFLOW 400 (F00012070)Fresenius Medical Care Renal Therapies Group, LLCK233213NxStage PureFlow SolutionNxstage Medical, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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