Pantera Pro
K 號：K160985 · 2016-10-07
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器材摘要
Pantera Pro is the device name listed in this FDA 510(k) record. The listed applicant is Biotronik, Inc.. It received FDA 510(k) clearance on 2016-10-07 under 510(k) number K160985. The device is classified under product code LOX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Pantera Pro?
Pantera Pro is a medical device that received FDA 510(k) clearance on 2016-10-07. The listed applicant is Biotronik, Inc.. The 510(k) number is K160985.
When did Pantera Pro receive FDA 510(k) clearance?
Pantera Pro received FDA 510(k) clearance on 2016-10-07, under 510(k) number K160985.
Who is the listed applicant for Pantera Pro?
The FDA 510(k) record lists Biotronik, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Pantera Pro?
The FDA product code for Pantera Pro is LOX.
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其他以 Biotronik, Inc. 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。
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相關器械（代碼：LOX）
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
在 FDA 資料庫中查看 →資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。
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