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FDA 510(k)

ENvizion醫療ENVue系統,ENvizion醫療腸內輸液管

K 號:K191387 · 2019-06-14

決定日期2019-06-14
產品代碼KNT
諮詢委員會GU
決定相當於

器材摘要

ENvizion Medical ENVue SYSTEM, ENvizion Medical Enteral Feeding Tube is the device name listed in this FDA 510(k) record. The listed applicant is Envizion Medical , Ltd.. It received FDA 510(k) clearance on 2019-06-14 under 510(k) number K191387. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the ENvizion Medical ENVue SYSTEM, ENvizion Medical Enteral Feeding Tube?

ENvizion Medical ENVue SYSTEM, ENvizion Medical Enteral Feeding Tube is a medical device that received FDA 510(k) clearance on 2019-06-14. The listed applicant is Envizion Medical , Ltd.. The 510(k) number is K191387.

When did ENvizion Medical ENVue SYSTEM, ENvizion Medical Enteral Feeding Tube receive FDA 510(k) clearance?

ENvizion Medical ENVue SYSTEM, ENvizion Medical Enteral Feeding Tube received FDA 510(k) clearance on 2019-06-14, under 510(k) number K191387.

Who is the listed applicant for ENvizion Medical ENVue SYSTEM, ENvizion Medical Enteral Feeding Tube?

The FDA 510(k) record lists Envizion Medical , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ENvizion Medical ENVue SYSTEM, ENvizion Medical Enteral Feeding Tube?

The FDA product code for ENvizion Medical ENVue SYSTEM, ENvizion Medical Enteral Feeding Tube is KNT.

相關臨床試驗

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其他以 Envizion Medical , Ltd. 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。

相關器械(代碼:KNT)

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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