FDA 510(k)

Kisses Mini

K号: K170394 · 2017-10-06

决定日期2017-10-06

产品代码DZE

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决定实质等同

器械摘要

Kisses Mini is the device name listed in this FDA 510(k) record. The listed applicant is Achimhai Medical Corporation. It received FDA 510(k) clearance on 2017-10-06 under 510(k) number K170394. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Kisses Mini?

Kisses Mini is a medical device that received FDA 510(k) clearance on 2017-10-06. The listed applicant is Achimhai Medical Corporation. The 510(k) number is K170394.

When did Kisses Mini receive FDA 510(k) clearance?

Kisses Mini received FDA 510(k) clearance on 2017-10-06, under 510(k) number K170394.

Who is the listed applicant for Kisses Mini?

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

What is the FDA product code for Kisses Mini?

The FDA product code for Kisses Mini is DZE.

列明Achimhai Medical 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。

K200193Kisses Plus 种植系统 K172630Kisses Plus 种植系统

官方来源

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