FDA 510(k)

MEG-TORQ

K 號：K161500 · 2017-02-22

決定日期2017-02-22

產品代碼EKX

諮詢委員會DE

決定相當於

器材摘要

MEG-TORQ is the device name listed in this FDA 510(k) record. The listed applicant is Micro-Nx Co., Ltd.. It received FDA 510(k) clearance on 2017-02-22 under 510(k) number K161500. The device is classified under product code EKX. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the MEG-TORQ?

MEG-TORQ is a medical device that received FDA 510(k) clearance on 2017-02-22. The listed applicant is Micro-Nx Co., Ltd.. The 510(k) number is K161500.

When did MEG-TORQ receive FDA 510(k) clearance?

MEG-TORQ received FDA 510(k) clearance on 2017-02-22, under 510(k) number K161500.

Who is the listed applicant for MEG-TORQ?

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

What is the FDA product code for MEG-TORQ?

The FDA product code for MEG-TORQ is EKX.

其他以 Micro-Nx Co., Ltd. 為申請人之記錄

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相關器械（代碼：EKX）

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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