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FDA 510(k)

WELL LIFE 无线经皮神经电刺激/电肌肉刺激器,型号 WR-2605/2605A

K号: K161453 · 2016-12-05

决定日期2016-12-05
产品代码NUH
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决定实质等同

器械摘要

WELL LIFE Wireless TENS/EMS Stimulator, Models WR-2605/2605A is the device name listed in this FDA 510(k) record. The listed applicant is Well-Life Healthcare Limited. It received FDA 510(k) clearance on 2016-12-05 under 510(k) number K161453. 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 WELL LIFE Wireless TENS/EMS Stimulator, Models WR-2605/2605A?

WELL LIFE Wireless TENS/EMS Stimulator, Models WR-2605/2605A is a medical device that received FDA 510(k) clearance on 2016-12-05. The listed applicant is Well-Life Healthcare Limited. The 510(k) number is K161453.

When did WELL LIFE Wireless TENS/EMS Stimulator, Models WR-2605/2605A receive FDA 510(k) clearance?

WELL LIFE Wireless TENS/EMS Stimulator, Models WR-2605/2605A received FDA 510(k) clearance on 2016-12-05, under 510(k) number K161453.

Who is the listed applicant for WELL LIFE Wireless TENS/EMS Stimulator, Models WR-2605/2605A?

The FDA 510(k) record lists Well-Life Healthcare Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WELL LIFE Wireless TENS/EMS Stimulator, Models WR-2605/2605A?

The FDA product code for WELL LIFE Wireless TENS/EMS Stimulator, Models WR-2605/2605A is NUH.

相关临床试验

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列明Well-Life Healthcare Limited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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