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FDA 510(k)

BioFire Global 還熱試劑板，BIOFIRE SHIELD 控制組合用於BioFire Global 還熱試劑板

K 號：K220870 · 2022-10-20

申請人Biofire Defense, LLC
決定日期2022-10-20
產品代碼QMV
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

BioFire Global Fever Panel, BIOFIRE SHIELD Control Kit for the BioFire Global Fever Panel is the device name listed in this FDA 510(k) record. The listed applicant is Biofire Defense, LLC. It received FDA 510(k) clearance on 2022-10-20 under 510(k) number K220870. The device is classified under product code QMV. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the BioFire Global Fever Panel, BIOFIRE SHIELD Control Kit for the BioFire Global Fever Panel?

BioFire Global Fever Panel, BIOFIRE SHIELD Control Kit for the BioFire Global Fever Panel is a medical device that received FDA 510(k) clearance on 2022-10-20. The listed applicant is Biofire Defense, LLC. The 510(k) number is K220870.

When did BioFire Global Fever Panel, BIOFIRE SHIELD Control Kit for the BioFire Global Fever Panel receive FDA 510(k) clearance?

BioFire Global Fever Panel, BIOFIRE SHIELD Control Kit for the BioFire Global Fever Panel received FDA 510(k) clearance on 2022-10-20, under 510(k) number K220870.

Who is the listed applicant for BioFire Global Fever Panel, BIOFIRE SHIELD Control Kit for the BioFire Global Fever Panel?

FDA 510(k) 記錄將 Biofire Defense, LLC 列為申請人。這並不單獨確立設備製造商。

What is the FDA product code for BioFire Global Fever Panel, BIOFIRE SHIELD Control Kit for the BioFire Global Fever Panel?

The FDA product code for BioFire Global Fever Panel, BIOFIRE SHIELD Control Kit for the BioFire Global Fever Panel is QMV.

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其他以 Biofire Defense, 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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查看所有 8 項裝置 →

相關器械（代碼：QMV）

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。

K243463BIOFIRE FILMARRAY 熱帶熱病面板Biofire Diagnostics, LLC (Biomerieux)

官方來源

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