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FDA 510(k)

FAQ™ (LED 面板);FAQ™ (双LED 面板)

K号: K253683 · 2026-02-20

申请人Foreo, Inc.
决定日期2026-02-20
产品代码OHS
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决定实质等同

器械摘要

FAQ™ (LED Panel); FAQ™ (Dual LED Panel) is the device name listed in this FDA 510(k) record. The listed applicant is Foreo, Inc.. It received FDA 510(k) clearance on 2026-02-20 under 510(k) number K253683. The device is classified under product code OHS. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the FAQ™ (LED Panel); FAQ™ (Dual LED Panel)?

FAQ™ (LED Panel); FAQ™ (Dual LED Panel) is a medical device that received FDA 510(k) clearance on 2026-02-20. The listed applicant is Foreo, Inc.. The 510(k) number is K253683.

When did FAQ™ (LED Panel); FAQ™ (Dual LED Panel) receive FDA 510(k) clearance?

FAQ™ (LED Panel); FAQ™ (Dual LED Panel) received FDA 510(k) clearance on 2026-02-20, under 510(k) number K253683.

Who is the listed applicant for FAQ™ (LED Panel); FAQ™ (Dual LED Panel)?

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

What is the FDA product code for FAQ™ (LED Panel); FAQ™ (Dual LED Panel)?

The FDA product code for FAQ™ (LED Panel); FAQ™ (Dual LED Panel) is OHS.

相关临床试验

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列明Foreo, 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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相关器械(代码:OHS)

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。

官方来源

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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。

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