FDA 510(k)

Monet凝固激光

K号: K201904 · 2020-11-24

决定日期2020-11-24

产品代码QNF

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决定实质等同

器械摘要

Monet Curing Laser is the device name listed in this FDA 510(k) record. The listed applicant is CAO Group, Inc.. It received FDA 510(k) clearance on 2020-11-24 under 510(k) number K201904. The device is classified under product code QNF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Monet Curing Laser?

Monet Curing Laser is a medical device that received FDA 510(k) clearance on 2020-11-24. The listed applicant is CAO Group, Inc.. The 510(k) number is K201904.

When did Monet Curing Laser receive FDA 510(k) clearance?

Monet Curing Laser received FDA 510(k) clearance on 2020-11-24, under 510(k) number K201904.

Who is the listed applicant for Monet Curing Laser?

The FDA 510(k) record lists CAO Group, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Monet Curing Laser?

The FDA product code for Monet Curing Laser is QNF.

列明CAO Group, Inc.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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