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FDA 510(k)

ARX Viral Transport Media Collection and Transport System

K-Number: K231843 · 2024-03-19

ApplicantArx Sciences, Inc.
Decision Date2024-03-19
Product CodeJSM
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

ARX Viral Transport Media Collection and Transport System is a medical device manufactured by Arx Sciences, Inc.. It received FDA 510(k) clearance on 2024-03-19 under approval 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. It is manufactured by Arx Sciences, Inc.. The 510(k) number is K231843.

When was ARX Viral Transport Media Collection and Transport System approved by the FDA?

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

What company makes ARX Viral Transport Media Collection and Transport System?

ARX Viral Transport Media Collection and Transport System is manufactured by Arx Sciences, Inc..

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.

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Related PubMed Literature

PMID: 41966529 Comparison of the AccuPower HIV-1 Quant Kit and Aptima HIV-1 Quant Dx Assay for quantification of HIV-1 plasma viral load. Diagnostic microbiology and infectious disease (2026)

Other Devices by Arx Sciences, Inc.

K222613ARX Liquid Amies Collection & Transport System

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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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