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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 the device name listed in this FDA 510(k) record. The listed applicant is Arx Sciences, Inc.. It received FDA 510(k) clearance on 2024-03-27 under 510(k) 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. The listed applicant is Arx Sciences, Inc.. The 510(k) number is K222613.

When did ARX Liquid Amies Collection & Transport System receive FDA 510(k) clearance?

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

Who is the listed applicant for ARX Liquid Amies Collection & Transport System?

The FDA 510(k) record lists Arx Sciences, Inc. as the applicant. This does not by itself establish the device manufacturer.

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.

Other records listing Arx Sciences, Inc. 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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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