FDA 510(k)

Accula Flu A/Flu B Test

K 號：K171641 · 2018-02-06

決定日期2018-02-06

產品代碼OZE

諮詢委員會MI (請提供完整的描述文本，以便進行翻譯。)

決定相當於

器材摘要

Accula Flu A/Flu B Test is the device name listed in this FDA 510(k) record. The listed applicant is Mesa Biotech, Inc.. It received FDA 510(k) clearance on 2018-02-06 under 510(k) number K171641. The device is classified under product code OZE. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Accula Flu A/Flu B Test?

Accula Flu A/Flu B Test is a medical device that received FDA 510(k) clearance on 2018-02-06. The listed applicant is Mesa Biotech, Inc.. The 510(k) number is K171641.

When did Accula Flu A/Flu B Test receive FDA 510(k) clearance?

Accula Flu A/Flu B Test received FDA 510(k) clearance on 2018-02-06, under 510(k) number K171641.

Who is the listed applicant for Accula Flu A/Flu B Test?

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

What is the FDA product code for Accula Flu A/Flu B Test?

The FDA product code for Accula Flu A/Flu B Test is OZE.

其他以 Mesa Biotech, Inc. 為申請人之記錄

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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相關器械（代碼：OZE）

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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