FDA 510(k)

AS-10

K 號：K200887 · 2020-04-15

決定日期2020-04-15

產品代碼OWB

諮詢委員會RA

決定相當於

器材摘要

AS-10 is the device name listed in this FDA 510(k) record. The listed applicant is Canon, Inc.. It received FDA 510(k) clearance on 2020-04-15 under 510(k) number K200887. The device is classified under product code OWB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the AS-10?

AS-10 is a medical device that received FDA 510(k) clearance on 2020-04-15. The listed applicant is Canon, Inc.. The 510(k) number is K200887.

When did AS-10 receive FDA 510(k) clearance?

AS-10 received FDA 510(k) clearance on 2020-04-15, under 510(k) number K200887.

Who is the listed applicant for AS-10?

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

What is the FDA product code for AS-10?

The FDA product code for AS-10 is OWB.

其他以 Canon, Inc. 為申請人之記錄

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相關器械（代碼：OWB）

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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