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FDA 510(k)

ARX Liquid Amies Collection & Transport System

K-Number: K222613 · 2024-03-27

ApplicantArx Sciences, Inc.
Decision Date2024-03-27
Product CodeLIO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

ARX Liquid Amies Collection & Transport System is a medical device manufactured by Arx Sciences, Inc.. It received FDA 510(k) clearance on 2024-03-27 under approval number K222613. The device is classified under product code LIO. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARX Liquid Amies Collection & Transport System?

ARX Liquid Amies Collection & Transport System is a medical device that received FDA 510(k) clearance on 2024-03-27. It is manufactured by Arx Sciences, Inc.. The 510(k) number is K222613.

When was ARX Liquid Amies Collection & Transport System approved by the FDA?

ARX Liquid Amies Collection & Transport System received FDA 510(k) clearance on 2024-03-27, under approval number K222613.

What company makes ARX Liquid Amies Collection & Transport System?

ARX Liquid Amies Collection & Transport System is manufactured by Arx Sciences, Inc..

What is the FDA product code for ARX Liquid Amies Collection & Transport System?

The FDA product code for ARX Liquid Amies Collection & Transport System is LIO.

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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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