FDA 510(k)

Videa牙周輔助

K 號：K223296 · 2023-02-06

決定日期2023-02-06

產品代碼QIH

諮詢委員會RA

決定相當於

器材摘要

Videa Perio Assist is the device name listed in this FDA 510(k) record. The listed applicant is Videahealth, Inc.. It received FDA 510(k) clearance on 2023-02-06 under 510(k) number K223296. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Videa Perio Assist?

Videa Perio Assist is a medical device that received FDA 510(k) clearance on 2023-02-06. The listed applicant is Videahealth, Inc.. The 510(k) number is K223296.

When did Videa Perio Assist receive FDA 510(k) clearance?

Videa Perio Assist received FDA 510(k) clearance on 2023-02-06, under 510(k) number K223296.

Who is the listed applicant for Videa Perio Assist?

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

What is the FDA product code for Videa Perio Assist?

The FDA product code for Videa Perio Assist is QIH.

其他以 Videahealth, Inc. 為申請人之記錄

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相關器械（代碼：QIH）

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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