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FDA 510(k)

Viz CTP

K-Number: K180161 · 2018-04-20

ApplicantViz. Ai, Inc.
Decision Date2018-04-20
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Viz CTP is a medical device manufactured by Viz. Ai, Inc.. It received FDA 510(k) clearance on 2018-04-20 under approval number K180161. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Viz CTP?

Viz CTP is a medical device that received FDA 510(k) clearance on 2018-04-20. It is manufactured by Viz. Ai, Inc.. The 510(k) number is K180161.

When was Viz CTP approved by the FDA?

Viz CTP received FDA 510(k) clearance on 2018-04-20, under approval number K180161.

What company makes Viz CTP?

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

What is the FDA product code for Viz CTP?

The FDA product code for Viz CTP is LLZ.

Other Devices by Viz. Ai, Inc.

K193658Viz ICH 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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