Fresenius Liberty Select Cycler
K-Number: K171652 · 2017-09-15
Decision Date2017-09-15
Product CodeFKX
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
Fresenius Liberty Select Cycler is a medical device manufactured by Fresenius Medical Care Renal Therapies Group, LLC. It received FDA 510(k) clearance on 2017-09-15 under approval 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. It is manufactured by Fresenius Medical Care Renal Therapies Group, LLC. The 510(k) number is K171652.
When was Fresenius Liberty Select Cycler approved by the FDA?
Fresenius Liberty Select Cycler received FDA 510(k) clearance on 2017-09-15, under approval number K171652.
What company makes Fresenius Liberty Select Cycler?
Fresenius Liberty Select Cycler is manufactured by Fresenius Medical Care Renal Therapies Group, LLC.
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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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.