FDA 510(k)

Activmotion S DTO

K 號：K202803 · 2021-12-16

決定日期2021-12-16

產品代碼HRS

諮詢委員會或

決定相當於

器材摘要

Activmotion S DTO is the device name listed in this FDA 510(k) record. The listed applicant is Newclip Technics. It received FDA 510(k) clearance on 2021-12-16 under 510(k) number K202803. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Activmotion S DTO?

Activmotion S DTO is a medical device that received FDA 510(k) clearance on 2021-12-16. The listed applicant is Newclip Technics. The 510(k) number is K202803.

When did Activmotion S DTO receive FDA 510(k) clearance?

Activmotion S DTO received FDA 510(k) clearance on 2021-12-16, under 510(k) number K202803.

Who is the listed applicant for Activmotion S DTO?

FDA 510(k) 記錄將 Newclip Technics 列為申請人。這並不單獨確立設備製造商。

What is the FDA product code for Activmotion S DTO?

The FDA product code for Activmotion S DTO is HRS.

其他以 Newclip Technics 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。

K261511Xpert 頸部 K261191Alians Elbow S K261038Xpert PFP K253906Xpert 手機械設備 K250767Newclip 患者匹配儀器非無菌 PSI K250155Xpert膝

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相關器械（代碼：HRS）

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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