Argus 认知 ReVISION 软件
K号: K223322 · 2023-07-24
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器械摘要
Argus Cognitive ReVISION Software is the device name listed in this FDA 510(k) record. The listed applicant is Argus Cognitive, Inc.. It received FDA 510(k) clearance on 2023-07-24 under 510(k) number K223322. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Argus Cognitive ReVISION Software?
Argus Cognitive ReVISION Software is a medical device that received FDA 510(k) clearance on 2023-07-24. The listed applicant is Argus Cognitive, Inc.. The 510(k) number is K223322.
When did Argus Cognitive ReVISION Software receive FDA 510(k) clearance?
Argus Cognitive ReVISION Software received FDA 510(k) clearance on 2023-07-24, under 510(k) number K223322.
Who is the listed applicant for Argus Cognitive ReVISION Software?
FDA 510(k)记录中列出Argus Cognitive, Inc.为申请人。这本身并不足以确立该设备制造商的身份。
What is the FDA product code for Argus Cognitive ReVISION Software?
The FDA product code for Argus Cognitive ReVISION Software is LLZ.
相关临床试验
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列明Argus Cognitive, Inc.为申报人的其他记录
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相关器械（代码：LLZ）
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。
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官方来源
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