INFX-8000C，V6.20
K 號：K152697 · 2016-01-15
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器材摘要
INFX-8000C, V6.20 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 2016-01-15 under 510(k) number K152697. 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 INFX-8000C, V6.20?
INFX-8000C, V6.20 is a medical device that received FDA 510(k) clearance on 2016-01-15. The listed applicant is Toshibamedical Systems Corporation. The 510(k) number is K152697.
When did INFX-8000C, V6.20 receive FDA 510(k) clearance?
INFX-8000C, V6.20 received FDA 510(k) clearance on 2016-01-15, under 510(k) number K152697.
Who is the listed applicant for INFX-8000C, V6.20?
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 INFX-8000C, V6.20?
The FDA product code for INFX-8000C, V6.20 is OWB.
其他以 Toshibamedical Systems Corporation 為申請人之記錄
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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
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