FDA 510(k)

橢圓Ydun

K 號：K180406 · 2018-03-15

決定日期2018-03-15

產品代碼GEX

諮詢委員會SU 請提供完整的描述文本，以便我進行翻譯。

決定相當於

器材摘要

Ellipse Ydun is the device name listed in this FDA 510(k) record. The listed applicant is Ellipse A/S. It received FDA 510(k) clearance on 2018-03-15 under 510(k) number K180406. The device is classified under product code GEX. It was reviewed by the SU advisory panel. Product code GEX falls under the category of Gastroenterology, which includes gastrointestinal diagnostic and therapeutic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

常見問題

What is the Ellipse Ydun?

Ellipse Ydun is a medical device that received FDA 510(k) clearance on 2018-03-15. The listed applicant is Ellipse A/S. The 510(k) number is K180406.

When did Ellipse Ydun receive FDA 510(k) clearance?

Ellipse Ydun received FDA 510(k) clearance on 2018-03-15, under 510(k) number K180406.

Who is the listed applicant for Ellipse Ydun?

The FDA 510(k) record lists Ellipse A/S as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Ellipse Ydun?

The FDA product code for Ellipse Ydun is GEX. This falls under the Gastroenterology category.

其他以 Ellipse A/S 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。

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相關器械（代碼：GEX）

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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