FDA 510(k)

Medi Lift PLUS

K号: K220198 · 2023-06-28

决定日期2023-06-28

产品代码NFO

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决定实质等同

器械摘要

Medi Lift PLUS is the device name listed in this FDA 510(k) record. The listed applicant is Ya-Man, Ltd.. It received FDA 510(k) clearance on 2023-06-28 under 510(k) number K220198. The device is classified under product code NFO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Medi Lift PLUS?

Medi Lift PLUS is a medical device that received FDA 510(k) clearance on 2023-06-28. The listed applicant is Ya-Man, Ltd.. The 510(k) number is K220198.

When did Medi Lift PLUS receive FDA 510(k) clearance?

Medi Lift PLUS received FDA 510(k) clearance on 2023-06-28, under 510(k) number K220198.

Who is the listed applicant for Medi Lift PLUS?

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

What is the FDA product code for Medi Lift PLUS?

The FDA product code for Medi Lift PLUS is NFO.

列明Ya-Man, 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。

K250618Medi Lift Essential 眼罩 K244048Medi Lift 面罩

官方来源

在 FDA 数据库中查看 →

数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。

器械摘要

常见问题

列明Ya-Man, Ltd.为申报人的其他记录

相关器械（代码：NFO）

官方来源