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FDA 510(k)

WS™ 远红外理疗单元,型号 KP-B210

K号: K160849 · 2016-12-15

决定日期2016-12-15
产品代码ILY
咨询委员会PM 请注意,由于您没有提供具体的医疗设备监管文本,我无法进行翻译。请提供具体的文本内容,以便我能够按照您的要求进行翻译。
决定实质等同

器械摘要

WS(TM) Far-Infrared Therapy Unit, Model KP-B210 is the device name listed in this FDA 510(k) record. The listed applicant is Ws Far IR Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2016-12-15 under 510(k) number K160849. The device is classified under product code ILY. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the WS(TM) Far-Infrared Therapy Unit, Model KP-B210?

WS(TM) Far-Infrared Therapy Unit, Model KP-B210 is a medical device that received FDA 510(k) clearance on 2016-12-15. The listed applicant is Ws Far IR Medical Technology Co., Ltd.. The 510(k) number is K160849.

When did WS(TM) Far-Infrared Therapy Unit, Model KP-B210 receive FDA 510(k) clearance?

WS(TM) Far-Infrared Therapy Unit, Model KP-B210 received FDA 510(k) clearance on 2016-12-15, under 510(k) number K160849.

Who is the listed applicant for WS(TM) Far-Infrared Therapy Unit, Model KP-B210?

The FDA 510(k) record lists Ws Far IR Medical Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WS(TM) Far-Infrared Therapy Unit, Model KP-B210?

The FDA product code for WS(TM) Far-Infrared Therapy Unit, Model KP-B210 is ILY.

相关临床试验

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相关器械(代码:ILY)

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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