TONOPORT VI
K 號：K170966 · 2017-06-14
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器材摘要
TONOPORT VI is the device name listed in this FDA 510(k) record. The listed applicant is Par Medizintechnik GmbH & Co. KG. It received FDA 510(k) clearance on 2017-06-14 under 510(k) number K170966. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the TONOPORT VI?
TONOPORT VI is a medical device that received FDA 510(k) clearance on 2017-06-14. The listed applicant is Par Medizintechnik GmbH & Co. KG. The 510(k) number is K170966.
When did TONOPORT VI receive FDA 510(k) clearance?
TONOPORT VI received FDA 510(k) clearance on 2017-06-14, under 510(k) number K170966.
Who is the listed applicant for TONOPORT VI?
The FDA 510(k) record lists Par Medizintechnik GmbH & Co. KG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TONOPORT VI?
The FDA product code for TONOPORT VI is DXN.
相關臨床試驗
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。
相關器械（代碼：DXN）
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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