FDA 510(k)

Viz LVO ContaCT

K号: K223042 · 2022-10-21

决定日期2022-10-21

产品代码QAS

咨询委员会RA

决定实质等同

器械摘要

Viz LVO ContaCT 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 2022-10-21 under 510(k) number K223042. The device is classified under product code QAS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Viz LVO ContaCT?

Viz LVO ContaCT is a medical device that received FDA 510(k) clearance on 2022-10-21. The listed applicant is Viz. Ai, Inc.. The 510(k) number is K223042.

When did Viz LVO ContaCT receive FDA 510(k) clearance?

Viz LVO ContaCT received FDA 510(k) clearance on 2022-10-21, under 510(k) number K223042.

Who is the listed applicant for Viz LVO ContaCT?

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 LVO ContaCT?

The FDA product code for Viz LVO ContaCT is QAS.

列明Viz. Ai, Inc.为申报人的其他记录

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。

K250354Viz Subdural+，Viz SUBDURAL PLUS K232363Viz HDS，Viz Volume Plus，Viz ICH+K223443Viz AAA K221100Viz RV/LV K220439Viz SDH K213319Viz 脑动脉瘤，Viz 焦虑

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