FDA 510(k)

Activmotion Range

K 號：K173746 · 2018-02-27

決定日期2018-02-27

產品代碼HRS

諮詢委員會或

決定相當於

器材摘要

Activmotion Range is the device name listed in this FDA 510(k) record. The listed applicant is Newclip Technics. It received FDA 510(k) clearance on 2018-02-27 under 510(k) number K173746. 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 Range?

Activmotion Range is a medical device that received FDA 510(k) clearance on 2018-02-27. The listed applicant is Newclip Technics. The 510(k) number is K173746.

When did Activmotion Range receive FDA 510(k) clearance?

Activmotion Range received FDA 510(k) clearance on 2018-02-27, under 510(k) number K173746.

Who is the listed applicant for Activmotion Range?

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 Range?

The FDA product code for Activmotion Range 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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