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FDA 510(k)

DR-HO's 背痛缓解系统 Pro(型号 BPRS-I 和 BPRS-II)

K号: K202671 · 2021-11-12

决定日期2021-11-12
产品代码NUH
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决定实质等同

器械摘要

DR-HO's Back Pain Relief System Pro (Models BPRS-I and BPRS-II) is the device name listed in this FDA 510(k) record. The listed applicant is Guangzhou Xinbo Electronic Co., Ltd.. It received FDA 510(k) clearance on 2021-11-12 under 510(k) number K202671. The device is classified under product code NUH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the DR-HO's Back Pain Relief System Pro (Models BPRS-I and BPRS-II)?

DR-HO's Back Pain Relief System Pro (Models BPRS-I and BPRS-II) is a medical device that received FDA 510(k) clearance on 2021-11-12. The listed applicant is Guangzhou Xinbo Electronic Co., Ltd.. The 510(k) number is K202671.

When did DR-HO's Back Pain Relief System Pro (Models BPRS-I and BPRS-II) receive FDA 510(k) clearance?

DR-HO's Back Pain Relief System Pro (Models BPRS-I and BPRS-II) received FDA 510(k) clearance on 2021-11-12, under 510(k) number K202671.

Who is the listed applicant for DR-HO's Back Pain Relief System Pro (Models BPRS-I and BPRS-II)?

The FDA 510(k) record lists Guangzhou Xinbo Electronic Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DR-HO's Back Pain Relief System Pro (Models BPRS-I and BPRS-II)?

The FDA product code for DR-HO's Back Pain Relief System Pro (Models BPRS-I and BPRS-II) is NUH.

相关临床试验

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列明Guangzhou Xinbo Electronic Co., Ltd.为申报人的其他记录

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相关器械(代码:NUH)

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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