FDA 510(k)

V80 麻醉蒸氣機（V80）

K 號：K240375 · 2024-10-31

申請人Shenzhen Mindray Bio-Medical Electronics Co., Ltd.

決定日期2024-10-31

產品代碼CAD

諮詢委員會AN

決定相當於

器材摘要

V80 Anesthetic Vaporizer (V80) is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Mindray Bio-Medical Electronics Co., Ltd.. It received FDA 510(k) clearance on 2024-10-31 under 510(k) number K240375. The device is classified under product code CAD. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the V80 Anesthetic Vaporizer (V80)?

V80 Anesthetic Vaporizer (V80) is a medical device that received FDA 510(k) clearance on 2024-10-31. The listed applicant is Shenzhen Mindray Bio-Medical Electronics Co., Ltd.. The 510(k) number is K240375.

When did V80 Anesthetic Vaporizer (V80) receive FDA 510(k) clearance?

V80 Anesthetic Vaporizer (V80) received FDA 510(k) clearance on 2024-10-31, under 510(k) number K240375.

Who is the listed applicant for V80 Anesthetic Vaporizer (V80)?

The FDA 510(k) record lists Shenzhen Mindray Bio-Medical Electronics Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for V80 Anesthetic Vaporizer (V80)?

The FDA product code for V80 Anesthetic Vaporizer (V80) is CAD.

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相關器械（代碼：CAD）

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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