FDA 510(k)

GingiKnit+、GingiBraid+ 和带有非浸渍退缩线的快捷连接

K号: K162164 · 2017-01-13

决定日期2017-01-13

产品代码MVL

决定实质等同

器械摘要

GingiKnit+, GingiBraid+, and Shortcut with GingiBraid+ Non-Impregnated Retraction Cord is the device name listed in this FDA 510(k) record. The listed applicant is Kerr Corporation. It received FDA 510(k) clearance on 2017-01-13 under 510(k) number K162164. The device is classified under product code MVL. FDA Decision: Substantially Equivalent.

常见问题

What is the GingiKnit+, GingiBraid+, and Shortcut with GingiBraid+ Non-Impregnated Retraction Cord?

GingiKnit+, GingiBraid+, and Shortcut with GingiBraid+ Non-Impregnated Retraction Cord is a medical device that received FDA 510(k) clearance on 2017-01-13. The listed applicant is Kerr Corporation. The 510(k) number is K162164.

When did GingiKnit+, GingiBraid+, and Shortcut with GingiBraid+ Non-Impregnated Retraction Cord receive FDA 510(k) clearance?

GingiKnit+, GingiBraid+, and Shortcut with GingiBraid+ Non-Impregnated Retraction Cord received FDA 510(k) clearance on 2017-01-13, under 510(k) number K162164.

Who is the listed applicant for GingiKnit+, GingiBraid+, and Shortcut with GingiBraid+ Non-Impregnated Retraction Cord?

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

What is the FDA product code for GingiKnit+, GingiBraid+, and Shortcut with GingiBraid+ Non-Impregnated Retraction Cord?

The FDA product code for GingiKnit+, GingiBraid+, and Shortcut with GingiBraid+ Non-Impregnated Retraction Cord is MVL.

列明Kerr Corporation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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