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FDA 510(k)

Viz ICH

K-Number: K193658 · 2020-03-18

ApplicantViz. Ai, Inc.
Decision Date2020-03-18
Product CodeQAS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Viz ICH is a medical device manufactured by Viz. Ai, Inc.. It received FDA 510(k) clearance on 2020-03-18 under approval number K193658. The device is classified under product code QAS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Viz ICH?

Viz ICH is a medical device that received FDA 510(k) clearance on 2020-03-18. It is manufactured by Viz. Ai, Inc.. The 510(k) number is K193658.

When was Viz ICH approved by the FDA?

Viz ICH received FDA 510(k) clearance on 2020-03-18, under approval number K193658.

What company makes Viz ICH?

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

What is the FDA product code for Viz ICH?

The FDA product code for Viz ICH is QAS.

Other Devices by Viz. Ai, Inc.

K180161Viz CTP K210209Viz ICH K223042Viz LVO ContaCT K221100Viz RV/LV K220439Viz SDH K213319Viz ANEURYSM, Viz ANX

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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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