FDA 510(k)

MADgic 喉氣管黏膜霧化裝置

K 號：K153470 · 2016-08-19

決定日期2016-08-19

產品代碼CCT

諮詢委員會AN

決定相當於

器材摘要

MADgic Laryngo-Tracheal Mucosal Atomization Device is the device name listed in this FDA 510(k) record. The listed applicant is Teleflex Medical. It received FDA 510(k) clearance on 2016-08-19 under 510(k) number K153470. The device is classified under product code CCT. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the MADgic Laryngo-Tracheal Mucosal Atomization Device?

MADgic Laryngo-Tracheal Mucosal Atomization Device is a medical device that received FDA 510(k) clearance on 2016-08-19. The listed applicant is Teleflex Medical. The 510(k) number is K153470.

When did MADgic Laryngo-Tracheal Mucosal Atomization Device receive FDA 510(k) clearance?

MADgic Laryngo-Tracheal Mucosal Atomization Device received FDA 510(k) clearance on 2016-08-19, under 510(k) number K153470.

Who is the listed applicant for MADgic Laryngo-Tracheal Mucosal Atomization Device?

FDA 510(k) 記錄將Teleflex Medical列為申請人。這並不單獨確立設備製造商的身份。

What is the FDA product code for MADgic Laryngo-Tracheal Mucosal Atomization Device?

The FDA product code for MADgic Laryngo-Tracheal Mucosal Atomization Device is CCT.

其他以 Teleflex Medical 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：CCT）

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。

K240114UltraEzAir® (UEA1A)Dualams, Inc., Dba Airkor K172956藥用黏膜噴霧器Medica Holdings, LLC

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