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FDA 510(k)

空气压力治疗系统

K号: K201935 · 2021-06-22

决定日期2021-06-22
产品代码IRP
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决定实质等同

器械摘要

Air Pressure Therapy System is the device name listed in this FDA 510(k) record. The listed applicant is Xiamen Weiyou Intelligent Technology Co., Ltd.. It received FDA 510(k) clearance on 2021-06-22 under 510(k) number K201935. The device is classified under product code IRP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Air Pressure Therapy System?

Air Pressure Therapy System is a medical device that received FDA 510(k) clearance on 2021-06-22. The listed applicant is Xiamen Weiyou Intelligent Technology Co., Ltd.. The 510(k) number is K201935.

When did Air Pressure Therapy System receive FDA 510(k) clearance?

Air Pressure Therapy System received FDA 510(k) clearance on 2021-06-22, under 510(k) number K201935.

Who is the listed applicant for Air Pressure Therapy System?

The FDA 510(k) record lists Xiamen Weiyou Intelligent Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Air Pressure Therapy System?

The FDA product code for Air Pressure Therapy System is IRP.

相关临床试验

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列明Xiamen Weiyou Intelligent Technology Co., Ltd.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。

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相关器械(代码:IRP)

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

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