FDA 510(k)

VentStar Resus 加熱式（N）（MP17030）；VentStar Autobreath 加熱式（N）（MP17031）

K 號：K242769 · 2025-04-04

決定日期2025-04-04

產品代碼BTL

諮詢委員會AN

決定相當於

器材摘要

VentStar Resus heated (N) (MP17030); VentStar Autobreath heated (N) (MP17031) is the device name listed in this FDA 510(k) record. The listed applicant is Draegerwerk AG & CO Kgaa. It received FDA 510(k) clearance on 2025-04-04 under 510(k) number K242769. The device is classified under product code BTL. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the VentStar Resus heated (N) (MP17030); VentStar Autobreath heated (N) (MP17031)?

VentStar Resus heated (N) (MP17030); VentStar Autobreath heated (N) (MP17031) is a medical device that received FDA 510(k) clearance on 2025-04-04. The listed applicant is Draegerwerk AG & CO Kgaa. The 510(k) number is K242769.

When did VentStar Resus heated (N) (MP17030); VentStar Autobreath heated (N) (MP17031) receive FDA 510(k) clearance?

VentStar Resus heated (N) (MP17030); VentStar Autobreath heated (N) (MP17031) received FDA 510(k) clearance on 2025-04-04, under 510(k) number K242769.

Who is the listed applicant for VentStar Resus heated (N) (MP17030); VentStar Autobreath heated (N) (MP17031)?

The FDA 510(k) record lists Draegerwerk AG & CO Kgaa as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VentStar Resus heated (N) (MP17030); VentStar Autobreath heated (N) (MP17031)?

The FDA product code for VentStar Resus heated (N) (MP17030); VentStar Autobreath heated (N) (MP17031) is BTL.

其他以 Draegerwerk AG & CO Kgaa 為申請人之記錄

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相關器械（代碼：BTL）

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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官方來源

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