FDA 510(k)

Midmark 頭外顯影系統 (EOIS)

K 號：K201667 · 2020-08-06

決定日期2020-08-06

產品代碼OAS

諮詢委員會RA

決定相當於

器材摘要

Midmark Extraoral Imaging System (EOIS) is the device name listed in this FDA 510(k) record. The listed applicant is Midmark Corporation. It received FDA 510(k) clearance on 2020-08-06 under 510(k) number K201667. The device is classified under product code OAS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Midmark Extraoral Imaging System (EOIS)?

Midmark Extraoral Imaging System (EOIS) is a medical device that received FDA 510(k) clearance on 2020-08-06. The listed applicant is Midmark Corporation. The 510(k) number is K201667.

When did Midmark Extraoral Imaging System (EOIS) receive FDA 510(k) clearance?

Midmark Extraoral Imaging System (EOIS) received FDA 510(k) clearance on 2020-08-06, under 510(k) number K201667.

Who is the listed applicant for Midmark Extraoral Imaging System (EOIS)?

The FDA 510(k) record lists Midmark Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Midmark Extraoral Imaging System (EOIS)?

The FDA product code for Midmark Extraoral Imaging System (EOIS) is OAS.

其他以 Midmark Corporation 為申請人之記錄

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相關器械（代碼：OAS）

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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