1717WCC / 1717WGC
K 號：K162519 · 2016-10-06
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器材摘要
1717WCC / 1717WGC is the device name listed in this FDA 510(k) record. The listed applicant is Rayence Co., Ltd.. It received FDA 510(k) clearance on 2016-10-06 under 510(k) number K162519. The device is classified under product code MQB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the 1717WCC / 1717WGC?
1717WCC / 1717WGC is a medical device that received FDA 510(k) clearance on 2016-10-06. The listed applicant is Rayence Co., Ltd.. The 510(k) number is K162519.
When did 1717WCC / 1717WGC receive FDA 510(k) clearance?
1717WCC / 1717WGC received FDA 510(k) clearance on 2016-10-06, under 510(k) number K162519.
Who is the listed applicant for 1717WCC / 1717WGC?
FDA 510(k) 記錄將 Rayence Co., Ltd. 列為申請人。這並不單獨確立設備製造商。
What is the FDA product code for 1717WCC / 1717WGC?
The FDA product code for 1717WCC / 1717WGC is MQB.
其他以 Rayence Co., Ltd. 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：MQB）
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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