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FDA 510(k)

KLS Martin 個人病人解決方案(IPS)規劃系統

K 號:K201052 · 2020-08-31

決定日期2020-08-31
產品代碼PPT
諮詢委員會NE (請提供完整的英文描述,以便進行翻譯。)
決定相當於

器材摘要

KLS Martin Individual Patient Solutions (IPS) Planning System is the device name listed in this FDA 510(k) record. The listed applicant is KLS-Martin L.P.. It received FDA 510(k) clearance on 2020-08-31 under 510(k) number K201052. The device is classified under product code PPT. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the KLS Martin Individual Patient Solutions (IPS) Planning System?

KLS Martin Individual Patient Solutions (IPS) Planning System is a medical device that received FDA 510(k) clearance on 2020-08-31. The listed applicant is KLS-Martin L.P.. The 510(k) number is K201052.

When did KLS Martin Individual Patient Solutions (IPS) Planning System receive FDA 510(k) clearance?

KLS Martin Individual Patient Solutions (IPS) Planning System received FDA 510(k) clearance on 2020-08-31, under 510(k) number K201052.

Who is the listed applicant for KLS Martin Individual Patient Solutions (IPS) Planning System?

FDA 510(k) 記錄將KLS-Martin L.P.列為申請人。這並不單獨確立設備製造商。

What is the FDA product code for KLS Martin Individual Patient Solutions (IPS) Planning System?

The FDA product code for KLS Martin Individual Patient Solutions (IPS) Planning System is PPT.

相關臨床試驗

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其他以 KLS-Martin L.P. 為申請人之記錄

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相關器械(代碼:PPT)

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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