FDA 510(k)

FilmArray 呼吸面板（RP）用於搭配 FilmArray Torch 使用

K 號：K160068 · 2016-02-08

決定日期2016-02-08

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

FilmArray Respiratory Panel (RP) for use with FilmArray Torch is the device name listed in this FDA 510(k) record. The listed applicant is Biofire Diagnostics, LLC. It received FDA 510(k) clearance on 2016-02-08 under 510(k) number K160068. 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 FilmArray Respiratory Panel (RP) for use with FilmArray Torch?

FilmArray Respiratory Panel (RP) for use with FilmArray Torch is a medical device that received FDA 510(k) clearance on 2016-02-08. The listed applicant is Biofire Diagnostics, LLC. The 510(k) number is K160068.

When did FilmArray Respiratory Panel (RP) for use with FilmArray Torch receive FDA 510(k) clearance?

FilmArray Respiratory Panel (RP) for use with FilmArray Torch received FDA 510(k) clearance on 2016-02-08, under 510(k) number K160068.

Who is the listed applicant for FilmArray Respiratory Panel (RP) for use with FilmArray Torch?

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

What is the FDA product code for FilmArray Respiratory Panel (RP) for use with FilmArray Torch?

The FDA product code for FilmArray Respiratory Panel (RP) for use with FilmArray Torch is OCC.

其他以 Biofire Diagnostics, LLC 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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