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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 the device name listed in this FDA 510(k) record. The listed applicant is Medo.Ai. It received FDA 510(k) clearance on 2020-06-11 under 510(k) 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. The listed applicant is Medo.Ai. The 510(k) number is K200356.

When did MEDO ARIA receive FDA 510(k) clearance?

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

Who is the listed applicant for MEDO ARIA?

The FDA 510(k) record lists Medo.Ai as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDO ARIA?

The FDA product code for MEDO ARIA is QIH.

Related Devices (Code: QIH)

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

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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