Infinix-i, INFX-8000V, V7.0
K 號：K172863 · 2017-12-14
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器材摘要
Infinix-i, INFX-8000V, V7.0 is the device name listed in this FDA 510(k) record. The listed applicant is Toshibamedical Systems Corporation. It received FDA 510(k) clearance on 2017-12-14 under 510(k) number K172863. The device is classified under product code OWB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Infinix-i, INFX-8000V, V7.0?
Infinix-i, INFX-8000V, V7.0 is a medical device that received FDA 510(k) clearance on 2017-12-14. The listed applicant is Toshibamedical Systems Corporation. The 510(k) number is K172863.
When did Infinix-i, INFX-8000V, V7.0 receive FDA 510(k) clearance?
Infinix-i, INFX-8000V, V7.0 received FDA 510(k) clearance on 2017-12-14, under 510(k) number K172863.
Who is the listed applicant for Infinix-i, INFX-8000V, V7.0?
The FDA 510(k) record lists Toshibamedical Systems Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Infinix-i, INFX-8000V, V7.0?
The FDA product code for Infinix-i, INFX-8000V, V7.0 is OWB.
相關臨床試驗
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其他以 Toshibamedical Systems Corporation 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。
相關器械（代碼：OWB）
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
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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