FDA 510(k)

BIOFIRE SPOTFIRE 呼吸 (R) 面板

K 號：K213954 · 2023-02-03

決定日期2023-02-03

產品代碼QOF

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 SPOTFIRE Respiratory (R) Panel is the device name listed in this FDA 510(k) record. The listed applicant is Biofire Diagnostics. It received FDA 510(k) clearance on 2023-02-03 under 510(k) number K213954. The device is classified under product code QOF. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the BIOFIRE SPOTFIRE Respiratory (R) Panel?

BIOFIRE SPOTFIRE Respiratory (R) Panel is a medical device that received FDA 510(k) clearance on 2023-02-03. The listed applicant is Biofire Diagnostics. The 510(k) number is K213954.

When did BIOFIRE SPOTFIRE Respiratory (R) Panel receive FDA 510(k) clearance?

BIOFIRE SPOTFIRE Respiratory (R) Panel received FDA 510(k) clearance on 2023-02-03, under 510(k) number K213954.

Who is the listed applicant for BIOFIRE SPOTFIRE Respiratory (R) Panel?

FDA 510(k) 記錄將 Biofire Diagnostics 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 SPOTFIRE Respiratory (R) Panel?

The FDA product code for BIOFIRE SPOTFIRE Respiratory (R) Panel is QOF.

其他以 Biofire Diagnostics 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。

K263054BIOFIRE 呼吸面板 2.1 (RP2.1)

相關器械（代碼：QOF）

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。

K261336Xpert 呼吸檢測組合Cepheid K263054BIOFIRE 呼吸面板 2.1 (RP2.1)Biofire Diagnostics K261837FINDER 流感A&B/SARS-CoV-2檢測Baebies, Inc.K252932快速PCR迷你呼吸道面板Autonomous Medical Devices Incorporated K252269FINDER 流感A&B/SARS-CoV-2檢測Baebies, Inc.K251742VELO 呼吸測試Lex Diagnostics Limited

官方來源

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