FDA 510(k)

Nutra Face Lift 模型 PE8050

K 號：K150826 · 2016-02-10

決定日期2016-02-10

產品代碼NFO

諮詢委員會NE (請提供完整的英文描述，以便進行翻譯。)

決定相當於

器材摘要

Nutra Face Lift Model PE8050 is the device name listed in this FDA 510(k) record. The listed applicant is Nutra Luxe MD, LLC. It received FDA 510(k) clearance on 2016-02-10 under 510(k) number K150826. The device is classified under product code NFO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Nutra Face Lift Model PE8050?

Nutra Face Lift Model PE8050 is a medical device that received FDA 510(k) clearance on 2016-02-10. The listed applicant is Nutra Luxe MD, LLC. The 510(k) number is K150826.

When did Nutra Face Lift Model PE8050 receive FDA 510(k) clearance?

Nutra Face Lift Model PE8050 received FDA 510(k) clearance on 2016-02-10, under 510(k) number K150826.

Who is the listed applicant for Nutra Face Lift Model PE8050?

The FDA 510(k) record lists Nutra Luxe MD, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Nutra Face Lift Model PE8050?

The FDA product code for Nutra Face Lift Model PE8050 is NFO.

其他以 Nutra Luxe MD, LLC 為申請人之記錄

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相關器械（代碼：NFO）

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。

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