FDA 510(k)

IU 嵌入系統

K 號：K172345 · 2018-06-18

決定日期2018-06-18

產品代碼DZE

諮詢委員會DE

決定相當於

器材摘要

IU Implant System is the device name listed in this FDA 510(k) record. The listed applicant is Warantec Co., Ltd.. It received FDA 510(k) clearance on 2018-06-18 under 510(k) number K172345. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the IU Implant System?

IU Implant System is a medical device that received FDA 510(k) clearance on 2018-06-18. The listed applicant is Warantec Co., Ltd.. The 510(k) number is K172345.

When did IU Implant System receive FDA 510(k) clearance?

IU Implant System received FDA 510(k) clearance on 2018-06-18, under 510(k) number K172345.

Who is the listed applicant for IU Implant System?

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

What is the FDA product code for IU Implant System?

The FDA product code for IU Implant System is DZE.

其他以 Warantec Co., 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。

K221972華安特客製牙橋 K221969IU植入系統基座

相關器械（代碼：DZE）

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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