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FDA 510(k)

ARX Viral Transport Media Collection and Transport System

K-Number: K231843 · 2024-03-19

Decision Date2024-03-19
Product CodeJSM
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

ARX Viral Transport Media Collection and 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 2024-03-19 under 510(k) number K231843. The device is classified under product code JSM. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARX Viral Transport Media Collection and Transport System?

ARX Viral Transport Media Collection and Transport System is a medical device that received FDA 510(k) clearance on 2024-03-19. The listed applicant is Arx Sciences, Inc.. The 510(k) number is K231843.

When did ARX Viral Transport Media Collection and Transport System receive FDA 510(k) clearance?

ARX Viral Transport Media Collection and Transport System received FDA 510(k) clearance on 2024-03-19, under 510(k) number K231843.

Who is the listed applicant for ARX Viral Transport Media Collection and 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 Viral Transport Media Collection and Transport System?

The FDA product code for ARX Viral Transport Media Collection and Transport System is JSM.

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.

Related Devices (Code: JSM)

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.

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.