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FDA 510(k)

Bonine按摩带

K号: K211823 · 2021-09-01

决定日期2021-09-01
产品代码MVV
决定实质等同

器械摘要

Bonine Acupressure Bands is the device name listed in this FDA 510(k) record. The listed applicant is Wellspring Pharmaceutical Corporation. It received FDA 510(k) clearance on 2021-09-01 under 510(k) number K211823. The device is classified under product code MVV. FDA Decision: Substantially Equivalent.

常见问题

What is the Bonine Acupressure Bands?

Bonine Acupressure Bands is a medical device that received FDA 510(k) clearance on 2021-09-01. The listed applicant is Wellspring Pharmaceutical Corporation. The 510(k) number is K211823.

When did Bonine Acupressure Bands receive FDA 510(k) clearance?

Bonine Acupressure Bands received FDA 510(k) clearance on 2021-09-01, under 510(k) number K211823.

Who is the listed applicant for Bonine Acupressure Bands?

The FDA 510(k) record lists Wellspring Pharmaceutical Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Bonine Acupressure Bands?

The FDA product code for Bonine Acupressure Bands is MVV.

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相关器械(代码:MVV)

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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