FDA 510(k)

BioFire戰士面板；BioFire戰士面板控制套件

K 號：K243822 · 2025-03-12

決定日期2025-03-12

產品代碼PRD

諮詢委員會此醫療器材為一項用於治療[疾病名稱]之裝置，已通過美國食品藥物管理局（FDA）之510(k)上市前通知程序，並取得[產品名稱]之上市許可。本裝置亦已獲得PMA（上市前核准）之認可，相關臨床試驗資料已登錄於ClinicalTrials.gov（NCT編號：[NCT號碼]），並已發表於經同儕審查之醫學期刊（PMID：[PMID號碼]）。更多詳細資訊請參閱：[URL]。

決定相當於

器材摘要

BioFire Warrior Panel; BioFire Warrior Panel Control Kit 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 2025-03-12 under 510(k) number K243822. The device is classified under product code PRD. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the BioFire Warrior Panel; BioFire Warrior Panel Control Kit?

BioFire Warrior Panel; BioFire Warrior Panel Control Kit is a medical device that received FDA 510(k) clearance on 2025-03-12. The listed applicant is Biofire Defense, LLC. The 510(k) number is K243822.

When did BioFire Warrior Panel; BioFire Warrior Panel Control Kit receive FDA 510(k) clearance?

BioFire Warrior Panel; BioFire Warrior Panel Control Kit received FDA 510(k) clearance on 2025-03-12, under 510(k) number K243822.

Who is the listed applicant for BioFire Warrior Panel; BioFire Warrior Panel Control Kit?

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 Warrior Panel; BioFire Warrior Panel Control Kit?

The FDA product code for BioFire Warrior Panel; BioFire Warrior Panel Control Kit is PRD.

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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相關器械（代碼：PRD）

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。

K170883FilmArray NGDS 戰士面板Biofire Defense, LLC

官方來源

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資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。