ThermoPro
K 號：K161862 · 2016-11-14
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器材摘要
ThermoPro is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer Medizinsysteme GmbH. It received FDA 510(k) clearance on 2016-11-14 under 510(k) number K161862. The device is classified under product code IMJ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the ThermoPro?
ThermoPro is a medical device that received FDA 510(k) clearance on 2016-11-14. The listed applicant is Zimmer Medizinsysteme GmbH. The 510(k) number is K161862.
When did ThermoPro receive FDA 510(k) clearance?
ThermoPro received FDA 510(k) clearance on 2016-11-14, under 510(k) number K161862.
Who is the listed applicant for ThermoPro?
The FDA 510(k) record lists Zimmer Medizinsysteme GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ThermoPro?
The FDA product code for ThermoPro is IMJ.
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其他以 Zimmer Medizinsysteme GmbH 為申請人之記錄
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相關器械（代碼：IMJ）
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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