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FDA 510(k)

AirLife 婴兒加熱線電路

K 號:K151303 · 2016-01-21

申請人Care Fusion
決定日期2016-01-21
產品代碼BZE
諮詢委員會AN
決定相當於

器材摘要

AirLife Infant Heated Wire Circuit is the device name listed in this FDA 510(k) record. The listed applicant is Care Fusion. It received FDA 510(k) clearance on 2016-01-21 under 510(k) number K151303. The device is classified under product code BZE. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the AirLife Infant Heated Wire Circuit?

AirLife Infant Heated Wire Circuit is a medical device that received FDA 510(k) clearance on 2016-01-21. The listed applicant is Care Fusion. The 510(k) number is K151303.

When did AirLife Infant Heated Wire Circuit receive FDA 510(k) clearance?

AirLife Infant Heated Wire Circuit received FDA 510(k) clearance on 2016-01-21, under 510(k) number K151303.

Who is the listed applicant for AirLife Infant Heated Wire Circuit?

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

What is the FDA product code for AirLife Infant Heated Wire Circuit?

The FDA product code for AirLife Infant Heated Wire Circuit is BZE.

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其他以 Care Fusion 為申請人之記錄

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相關器械(代碼:BZE)

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。

官方來源

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