Hi-Dow Wireless TENS/EMS System (Model HD-5N)
K号: K163393 · 2017-08-04
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器械摘要
常见问题
What is the Hi-Dow Wireless TENS/EMS System (Model HD-5N)?
Hi-Dow Wireless TENS/EMS System (Model HD-5N) is a medical device that received FDA 510(k) clearance on 2017-08-04. The listed applicant is Hi-Dow International, Inc.. The 510(k) number is K163393.
When did Hi-Dow Wireless TENS/EMS System (Model HD-5N) receive FDA 510(k) clearance?
Hi-Dow Wireless TENS/EMS System (Model HD-5N) received FDA 510(k) clearance on 2017-08-04, under 510(k) number K163393.
Who is the listed applicant for Hi-Dow Wireless TENS/EMS System (Model HD-5N)?
The FDA 510(k) record lists Hi-Dow International, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Hi-Dow Wireless TENS/EMS System (Model HD-5N)?
The FDA product code for Hi-Dow Wireless TENS/EMS System (Model HD-5N) is NUH.
相关临床试验
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列明Hi-Dow International, Inc.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
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。
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