FDA 510(k)

MU2net

K 號：K191944 · 2019-10-24

決定日期2019-10-24

產品代碼IYE

諮詢委員會RA

決定相當於

器材摘要

MU2net is the device name listed in this FDA 510(k) record. The listed applicant is Dosisoft. It received FDA 510(k) clearance on 2019-10-24 under 510(k) number K191944. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the MU2net?

MU2net is a medical device that received FDA 510(k) clearance on 2019-10-24. The listed applicant is Dosisoft. The 510(k) number is K191944.

When did MU2net receive FDA 510(k) clearance?

MU2net received FDA 510(k) clearance on 2019-10-24, under 510(k) number K191944.

Who is the listed applicant for MU2net?

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

What is the FDA product code for MU2net?

The FDA product code for MU2net is IYE.

其他以 Dosisoft 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：IYE）

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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