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FDA 510(k)

Alio

K-Number: K223073 · 2023-03-17

ApplicantAlio, Inc.
Decision Date2023-03-17
Product CodeDRG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Alio is a medical device manufactured by Alio, Inc.. It received FDA 510(k) clearance on 2023-03-17 under approval number K223073. The device is classified under product code DRG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Alio?

Alio is a medical device that received FDA 510(k) clearance on 2023-03-17. It is manufactured by Alio, Inc.. The 510(k) number is K223073.

When was Alio approved by the FDA?

Alio received FDA 510(k) clearance on 2023-03-17, under approval number K223073.

What company makes Alio?

Alio is manufactured by Alio, Inc..

What is the FDA product code for Alio?

The FDA product code for Alio is DRG.

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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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