CloudVue
K号: K203058 · 2020-10-29
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器械摘要
CloudVue is the device name listed in this FDA 510(k) record. The listed applicant is International Medical Solutions, Inc.. It received FDA 510(k) clearance on 2020-10-29 under 510(k) number K203058. 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 CloudVue?
CloudVue is a medical device that received FDA 510(k) clearance on 2020-10-29. The listed applicant is International Medical Solutions, Inc.. The 510(k) number is K203058.
When did CloudVue receive FDA 510(k) clearance?
CloudVue received FDA 510(k) clearance on 2020-10-29, under 510(k) number K203058.
Who is the listed applicant for CloudVue?
The FDA 510(k) record lists International Medical Solutions, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CloudVue?
The FDA product code for CloudVue is LLZ.
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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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