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FDA 510(k)

MEDO ARIA

K-Number: K200356 · 2020-06-11

ApplicantMedo.Ai
Decision Date2020-06-11
Product CodeQIH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MEDO ARIA is a medical device manufactured by Medo.Ai. It received FDA 510(k) clearance on 2020-06-11 under approval number K200356. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDO ARIA?

MEDO ARIA is a medical device that received FDA 510(k) clearance on 2020-06-11. It is manufactured by Medo.Ai. The 510(k) number is K200356.

When was MEDO ARIA approved by the FDA?

MEDO ARIA received FDA 510(k) clearance on 2020-06-11, under approval number K200356.

What company makes MEDO ARIA?

MEDO ARIA is manufactured by Medo.Ai.

What is the FDA product code for MEDO ARIA?

The FDA product code for MEDO ARIA is QIH.

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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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