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FDA 510(k)

Careflux H60;Careflux H70;Careflux V500

K-Number: K261267 · 2026-07-24

ApplicantFresenius Medical Care Renal Therapies Group, LLC
Decision Date2026-07-24
Product CodeKDI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Careflux H60;Careflux H70;Careflux V500 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 2026-07-24 under 510(k) number K261267. The device is classified under product code KDI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Careflux H60;Careflux H70;Careflux V500?

Careflux H60;Careflux H70;Careflux V500 is a medical device that received FDA 510(k) clearance on 2026-07-24. The listed applicant is Fresenius Medical Care Renal Therapies Group, LLC. The 510(k) number is K261267.

When did Careflux H60;Careflux H70;Careflux V500 receive FDA 510(k) clearance?

Careflux H60;Careflux H70;Careflux V500 received FDA 510(k) clearance on 2026-07-24, under 510(k) number K261267.

Who is the listed applicant for Careflux H60;Careflux H70;Careflux V500?

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 Careflux H60;Careflux H70;Careflux V500?

The FDA product code for Careflux H60;Careflux H70;Careflux V500 is KDI.

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

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.

K252377NxStage System One with NxViewK252459multiFlux 130 (F00013123); multiFlux 160 (F00013124)K253462NaturaLyte® Dry Bicarbonate Concentrate (08-4112-2)K253518FX CorAL 40; FX CorAL 50K250634BCM2-Body Composition MonitorK250471AquaC UNO H

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Related Devices (Code: KDI)

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.

K252377NxStage System One with NxViewFresenius Medical Care Renal Therapies Group, LLCK260533ELISIO™-HNipro Medical CorporationK252459multiFlux 130 (F00013123); multiFlux 160 (F00013124)Fresenius Medical Care Renal Therapies Group, LLCK253412Tablo Hemodialysis System (PN-0008000, PN-0006000U)Outset Medical, Inc.K253518FX CorAL 40; FX CorAL 50Fresenius Medical Care Renal Therapies Group, LLCK243920Purema H Hemoconcentrator - PediatricMedica USA, 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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