Viz SDH
K号: K220439 · 2022-07-25
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器械摘要
Viz SDH 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 2022-07-25 under 510(k) number K220439. 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 SDH?
Viz SDH is a medical device that received FDA 510(k) clearance on 2022-07-25. The listed applicant is Viz. Ai, Inc.. The 510(k) number is K220439.
When did Viz SDH receive FDA 510(k) clearance?
Viz SDH received FDA 510(k) clearance on 2022-07-25, under 510(k) number K220439.
Who is the listed applicant for Viz SDH?
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 SDH?
The FDA product code for Viz SDH 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。
相关器械（代码：QAS）
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。
官方来源
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。
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