FDA 510(k)

Avologi Gel Primer (型號：Av25)

K 號：K220735 · 2023-09-15

決定日期2023-09-15

產品代碼GYB

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

Avologi Gel Primer (Model: Av25) is the device name listed in this FDA 510(k) record. The listed applicant is Premier North America, Inc.. It received FDA 510(k) clearance on 2023-09-15 under 510(k) number K220735. The device is classified under product code GYB. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Avologi Gel Primer (Model: Av25)?

Avologi Gel Primer (Model: Av25) is a medical device that received FDA 510(k) clearance on 2023-09-15. The listed applicant is Premier North America, Inc.. The 510(k) number is K220735.

When did Avologi Gel Primer (Model: Av25) receive FDA 510(k) clearance?

Avologi Gel Primer (Model: Av25) received FDA 510(k) clearance on 2023-09-15, under 510(k) number K220735.

Who is the listed applicant for Avologi Gel Primer (Model: Av25)?

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

What is the FDA product code for Avologi Gel Primer (Model: Av25)?

The FDA product code for Avologi Gel Primer (Model: Av25) is GYB.

其他以 Premier North America, Inc. 為申請人之記錄

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相關器械（代碼：GYB）

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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