FDA 510(k)

AeroNOx 2.0 一氧化氮滴定與監測系統

K 號：K193481 · 2020-03-10

決定日期2020-03-10

產品代碼MRN

諮詢委員會AN

決定相當於

器材摘要

AeroNOx 2.0 Nitric Oxide Titration & Monitoring System is the device name listed in this FDA 510(k) record. The listed applicant is International Biomedical. It received FDA 510(k) clearance on 2020-03-10 under 510(k) number K193481. The device is classified under product code MRN. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the AeroNOx 2.0 Nitric Oxide Titration & Monitoring System?

AeroNOx 2.0 Nitric Oxide Titration & Monitoring System is a medical device that received FDA 510(k) clearance on 2020-03-10. The listed applicant is International Biomedical. The 510(k) number is K193481.

When did AeroNOx 2.0 Nitric Oxide Titration & Monitoring System receive FDA 510(k) clearance?

AeroNOx 2.0 Nitric Oxide Titration & Monitoring System received FDA 510(k) clearance on 2020-03-10, under 510(k) number K193481.

Who is the listed applicant for AeroNOx 2.0 Nitric Oxide Titration & Monitoring System?

The FDA 510(k) record lists International Biomedical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AeroNOx 2.0 Nitric Oxide Titration & Monitoring System?

The FDA product code for AeroNOx 2.0 Nitric Oxide Titration & Monitoring System is MRN.

其他以 International Biomedical 為申請人之記錄

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相關器械（代碼：MRN）

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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