IP轉換器
K 號：K191678 · 2020-01-10
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器材摘要
IP Converter is the device name listed in this FDA 510(k) record. The listed applicant is Sony Electronics, Inc.. It received FDA 510(k) clearance on 2020-01-10 under 510(k) number K191678. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the IP Converter?
IP Converter is a medical device that received FDA 510(k) clearance on 2020-01-10. The listed applicant is Sony Electronics, Inc.. The 510(k) number is K191678.
When did IP Converter receive FDA 510(k) clearance?
IP Converter received FDA 510(k) clearance on 2020-01-10, under 510(k) number K191678.
Who is the listed applicant for IP Converter?
The FDA 510(k) record lists Sony Electronics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for IP Converter?
The FDA product code for IP Converter is GCJ.
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其他以 Sony Electronics, 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。
相關器械（代碼：GCJ）
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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