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FDA 510(k)

iStim S2非处方OTC疼痛缓解经皮神经电刺激器

K号: K181849 · 2018-08-10

决定日期2018-08-10
产品代码NUH
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决定实质等同

器械摘要

iStim S2 OTC Pain Relief TENS is the device name listed in this FDA 510(k) record. The listed applicant is Everyway Medical Instruments Co., Ldt.. It received FDA 510(k) clearance on 2018-08-10 under 510(k) number K181849. 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 iStim S2 OTC Pain Relief TENS?

iStim S2 OTC Pain Relief TENS is a medical device that received FDA 510(k) clearance on 2018-08-10. The listed applicant is Everyway Medical Instruments Co., Ldt.. The 510(k) number is K181849.

When did iStim S2 OTC Pain Relief TENS receive FDA 510(k) clearance?

iStim S2 OTC Pain Relief TENS received FDA 510(k) clearance on 2018-08-10, under 510(k) number K181849.

Who is the listed applicant for iStim S2 OTC Pain Relief TENS?

The FDA 510(k) record lists Everyway Medical Instruments Co., Ldt. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for iStim S2 OTC Pain Relief TENS?

The FDA product code for iStim S2 OTC Pain Relief TENS is NUH.

相关临床试验

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列明Everyway Medical Instruments Co., Ldt.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

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