可见患者套件
K号: K212896 · 2021-11-05
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器械摘要
Visible Patient Suite is the device name listed in this FDA 510(k) record. The listed applicant is Visible Patient, Sas. It received FDA 510(k) clearance on 2021-11-05 under 510(k) number K212896. 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 Visible Patient Suite?
Visible Patient Suite is a medical device that received FDA 510(k) clearance on 2021-11-05. The listed applicant is Visible Patient, Sas. The 510(k) number is K212896.
When did Visible Patient Suite receive FDA 510(k) clearance?
Visible Patient Suite received FDA 510(k) clearance on 2021-11-05, under 510(k) number K212896.
Who is the listed applicant for Visible Patient Suite?
The FDA 510(k) record lists Visible Patient, Sas as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Visible Patient Suite?
The FDA product code for Visible Patient Suite is LLZ.
相关临床试验
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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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