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FDA 510(k)

Viz AAA

K-Number: K223443 · 2023-03-17

ApplicantViz. Ai, Inc.
Decision Date2023-03-17
Product CodeQFM
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Viz AAA is a medical device manufactured by Viz. Ai, Inc.. It received FDA 510(k) clearance on 2023-03-17 under approval number K223443. The device is classified under product code QFM. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Viz AAA?

Viz AAA is a medical device that received FDA 510(k) clearance on 2023-03-17. It is manufactured by Viz. Ai, Inc.. The 510(k) number is K223443.

When was Viz AAA approved by the FDA?

Viz AAA received FDA 510(k) clearance on 2023-03-17, under approval number K223443.

What company makes Viz AAA?

Viz AAA is manufactured by Viz. Ai, Inc..

What is the FDA product code for Viz AAA?

The FDA product code for Viz AAA is QFM.

Other Devices by Viz. Ai, Inc.

K180161Viz CTP K193658Viz ICH K210209Viz ICH K223042Viz LVO ContaCT K221100Viz RV/LV K220439Viz SDH

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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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