FDA 510(k)空气压力足部按摩器
K号: K212935 · 2022-02-19
决定日期2022-02-19
产品代码IRP
咨询委员会PM
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决定实质等同
器械摘要
Air Pressure Foot Massager is the device name listed in this FDA 510(k) record. The listed applicant is Xiamen Simo Electronic Co., Ltd.. It received FDA 510(k) clearance on 2022-02-19 under 510(k) number K212935. 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 Foot Massager?
Air Pressure Foot Massager is a medical device that received FDA 510(k) clearance on 2022-02-19. The listed applicant is Xiamen Simo Electronic Co., Ltd.. The 510(k) number is K212935.
When did Air Pressure Foot Massager receive FDA 510(k) clearance?
Air Pressure Foot Massager received FDA 510(k) clearance on 2022-02-19, under 510(k) number K212935.
Who is the listed applicant for Air Pressure Foot Massager?
The FDA 510(k) record lists Xiamen Simo Electronic Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Air Pressure Foot Massager?
The FDA product code for Air Pressure Foot Massager is IRP.
相关临床试验
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: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。
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