FDA 510(k)

スマートアプリガイドド™ マイクロカレントフェイスマリフトペン 6 in 1

K番号: K250361 · 2025-05-23

決定日2025-05-23

製品コードNFO

諮問委員会Please provide the source text to translate.

決定大幅同等

医療機器の概要

SmartAppGuidedTM MicroCurrent Face-Lift Pen 6 in 1 is the device name listed in this FDA 510(k) record. The listed applicant is Geske Beauty Tech GmbH. It received FDA 510(k) clearance on 2025-05-23 under 510(k) number K250361. The device is classified under product code NFO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

よくある質問

What is the SmartAppGuidedTM MicroCurrent Face-Lift Pen 6 in 1?

SmartAppGuidedTM MicroCurrent Face-Lift Pen 6 in 1 is a medical device that received FDA 510(k) clearance on 2025-05-23. The listed applicant is Geske Beauty Tech GmbH. The 510(k) number is K250361.

When did SmartAppGuidedTM MicroCurrent Face-Lift Pen 6 in 1 receive FDA 510(k) clearance?

SmartAppGuidedTM MicroCurrent Face-Lift Pen 6 in 1 received FDA 510(k) clearance on 2025-05-23, under 510(k) number K250361.

Who is the listed applicant for SmartAppGuidedTM MicroCurrent Face-Lift Pen 6 in 1?

The FDA 510(k) record lists Geske Beauty Tech GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SmartAppGuidedTM MicroCurrent Face-Lift Pen 6 in 1?

The FDA product code for SmartAppGuidedTM MicroCurrent Face-Lift Pen 6 in 1 is NFO.

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スマートアプリガイドド™ マイクロカレントフェイスマリフトペン 6 in 1

医療機器の概要

よくある質問

関連する臨床試験

関連機器（コード：NFO）

公式ソース