動態校正系統
K 號：K193324 · 2020-02-04
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器材摘要
Motion Correction System is the device name listed in this FDA 510(k) record. The listed applicant is Kineticor, Inc.. It received FDA 510(k) clearance on 2020-02-04 under 510(k) number K193324. 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 Motion Correction System?
Motion Correction System is a medical device that received FDA 510(k) clearance on 2020-02-04. The listed applicant is Kineticor, Inc.. The 510(k) number is K193324.
When did Motion Correction System receive FDA 510(k) clearance?
Motion Correction System received FDA 510(k) clearance on 2020-02-04, under 510(k) number K193324.
Who is the listed applicant for Motion Correction System?
The FDA 510(k) record lists Kineticor, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Motion Correction System?
The FDA product code for Motion Correction System is LNH.
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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。
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官方來源
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