FDA 510(k)

Viz CTP

K-Number: K180161 · 2018-04-20

Decision Date2018-04-20

Product CodeLLZ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

Viz CTP is the device name listed in this FDA 510(k) record. The listed applicant is Viz. Ai, Inc.. It received FDA 510(k) clearance on 2018-04-20 under 510(k) 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. The listed applicant is Viz. Ai, Inc.. The 510(k) number is K180161.

When did Viz CTP receive FDA 510(k) clearance?

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

Who is the listed applicant for Viz CTP?

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

What is the FDA product code for Viz CTP?

The FDA product code for Viz CTP is LLZ.

Other records listing Viz. Ai, Inc. as applicant

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.