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FDA 510(k)

TCL3 運動追蹤系統

K 號:K203451 · 2021-04-28

決定日期2021-04-28
產品代碼LNH
諮詢委員會RA
決定相當於

器材摘要

TCL3 Motion Tracking System is the device name listed in this FDA 510(k) record. The listed applicant is Tracinnovations Aps. It received FDA 510(k) clearance on 2021-04-28 under 510(k) number K203451. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the TCL3 Motion Tracking System?

TCL3 Motion Tracking System is a medical device that received FDA 510(k) clearance on 2021-04-28. The listed applicant is Tracinnovations Aps. The 510(k) number is K203451.

When did TCL3 Motion Tracking System receive FDA 510(k) clearance?

TCL3 Motion Tracking System received FDA 510(k) clearance on 2021-04-28, under 510(k) number K203451.

Who is the listed applicant for TCL3 Motion Tracking System?

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

What is the FDA product code for TCL3 Motion Tracking System?

The FDA product code for TCL3 Motion Tracking System is LNH.

相關臨床試驗

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相關器械(代碼:LNH)

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。

官方來源

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