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FDA 510(k)

Fresenius Liberty Select Cycler

K-Number: K171652 · 2017-09-15

ApplicantFresenius Medical Care Renal Therapies Group, LLC
Decision Date2017-09-15
Product CodeFKX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Fresenius Liberty Select Cycler 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 2017-09-15 under 510(k) number K171652. The device is classified under product code FKX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Fresenius Liberty Select Cycler?

Fresenius Liberty Select Cycler is a medical device that received FDA 510(k) clearance on 2017-09-15. The listed applicant is Fresenius Medical Care Renal Therapies Group, LLC. The 510(k) number is K171652.

When did Fresenius Liberty Select Cycler receive FDA 510(k) clearance?

Fresenius Liberty Select Cycler received FDA 510(k) clearance on 2017-09-15, under 510(k) number K171652.

Who is the listed applicant for Fresenius Liberty Select Cycler?

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 Fresenius Liberty Select Cycler?

The FDA product code for Fresenius Liberty Select Cycler is FKX.

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Related Devices (Code: FKX)

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.

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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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