GR40CW
K 號：K181631 · 2018-07-20
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器材摘要
GR40CW is the device name listed in this FDA 510(k) record. The listed applicant is Samsung Electronics Co., Ltd.. It received FDA 510(k) clearance on 2018-07-20 under 510(k) number K181631. 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 GR40CW?
GR40CW is a medical device that received FDA 510(k) clearance on 2018-07-20. The listed applicant is Samsung Electronics Co., Ltd.. The 510(k) number is K181631.
When did GR40CW receive FDA 510(k) clearance?
GR40CW received FDA 510(k) clearance on 2018-07-20, under 510(k) number K181631.
Who is the listed applicant for GR40CW?
FDA 510(k) 記錄將三星電子有限公司列為申請人。這並不單獨確立設備製造商。
What is the FDA product code for GR40CW?
The FDA product code for GR40CW is MQB.
其他以 Samsung Electronics Co., Ltd. 為申請人之記錄
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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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