DR-HO's 背痛缓解系统 Pro(型号 BPRS-I 和 BPRS-II)
K号: K202671 · 2021-11-12
广告
器械摘要
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
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。
列明Guangzhou Xinbo Electronic 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。
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
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息,请务必参考官方记录。
广告