FDA 510(k)

磁力奧斯易打包膠泥

K 號：K211201 · 2021-09-02

決定日期2021-09-02

產品代碼MQV

諮詢委員會或

決定相當於

器材摘要

MagnetOs Easypack Putty is the device name listed in this FDA 510(k) record. The listed applicant is Kuros Biosciences B.V. It received FDA 510(k) clearance on 2021-09-02 under 510(k) number K211201. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the MagnetOs Easypack Putty?

MagnetOs Easypack Putty is a medical device that received FDA 510(k) clearance on 2021-09-02. The listed applicant is Kuros Biosciences B.V. The 510(k) number is K211201.

When did MagnetOs Easypack Putty receive FDA 510(k) clearance?

MagnetOs Easypack Putty received FDA 510(k) clearance on 2021-09-02, under 510(k) number K211201.

Who is the listed applicant for MagnetOs Easypack Putty?

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

What is the FDA product code for MagnetOs Easypack Putty?

The FDA product code for MagnetOs Easypack Putty is MQV.

其他以 Kuros Biosciences B.V 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：MQV）

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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