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FDA 510(k)

FRESENIUS LIBERTY CYCLER

K-Number: K043363 · 2005-03-31

ApplicantFresenius Medical Care North America
Decision Date2005-03-31
Product CodeFKX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

FRESENIUS LIBERTY CYCLER is the device name listed in this FDA 510(k) record. The listed applicant is Fresenius Medical Care North America. It received FDA 510(k) clearance on 2005-03-31 under 510(k) number K043363. 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 CYCLER?

FRESENIUS LIBERTY CYCLER is a medical device that received FDA 510(k) clearance on 2005-03-31. The listed applicant is Fresenius Medical Care North America. The 510(k) number is K043363.

When did FRESENIUS LIBERTY CYCLER receive FDA 510(k) clearance?

FRESENIUS LIBERTY CYCLER received FDA 510(k) clearance on 2005-03-31, under 510(k) number K043363.

Who is the listed applicant for FRESENIUS LIBERTY CYCLER?

The FDA 510(k) record lists Fresenius Medical Care North America as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FRESENIUS LIBERTY CYCLER?

The FDA product code for FRESENIUS LIBERTY CYCLER is FKX.

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Other records listing Fresenius Medical Care North America as applicant

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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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