FDA 510(k)

Accula RSV Test

K 號：K181443 · 2018-11-23

決定日期2018-11-23

產品代碼OCC

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 RSV 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 2018-11-23 under 510(k) number K181443. The device is classified under product code OCC. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Accula RSV Test?

Accula RSV Test is a medical device that received FDA 510(k) clearance on 2018-11-23. The listed applicant is Mesa Biotech, Inc.. The 510(k) number is K181443.

When did Accula RSV Test receive FDA 510(k) clearance?

Accula RSV Test received FDA 510(k) clearance on 2018-11-23, under 510(k) number K181443.

Who is the listed applicant for Accula RSV 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 RSV Test?

The FDA product code for Accula RSV Test is OCC.

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：OCC）

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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官方來源

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