FDA 510(k)

V-瓦森斯高级

K号: K160377 · 2016-12-02

决定日期2016-12-02

产品代码LBH

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决定实质等同

器械摘要

V-varnish Premium is the device name listed in this FDA 510(k) record. The listed applicant is Vericom Co., Ltd.. It received FDA 510(k) clearance on 2016-12-02 under 510(k) number K160377. The device is classified under product code LBH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the V-varnish Premium?

V-varnish Premium is a medical device that received FDA 510(k) clearance on 2016-12-02. The listed applicant is Vericom Co., Ltd.. The 510(k) number is K160377.

When did V-varnish Premium receive FDA 510(k) clearance?

V-varnish Premium received FDA 510(k) clearance on 2016-12-02, under 510(k) number K160377.

Who is the listed applicant for V-varnish Premium?

The FDA 510(k) record lists Vericom Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for V-varnish Premium?

The FDA product code for V-varnish Premium is LBH.

列明Vericom 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。

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官方来源

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