樓福康矽膠泡沫敷料
K 號：K160022 · 2016-08-17
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器材摘要
LUOFUCON Silicone Ag foam dressing is the device name listed in this FDA 510(k) record. The listed applicant is Huizhou Foryou Medical Devices Co., Ltd.. It received FDA 510(k) clearance on 2016-08-17 under 510(k) number K160022. The device is classified under product code FRO. Product code FRO falls under the category of Anesthesiology, which includes devices for anesthetic delivery and patient monitoring. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.
常見問題
What is the LUOFUCON Silicone Ag foam dressing?
LUOFUCON Silicone Ag foam dressing is a medical device that received FDA 510(k) clearance on 2016-08-17. The listed applicant is Huizhou Foryou Medical Devices Co., Ltd.. The 510(k) number is K160022.
When did LUOFUCON Silicone Ag foam dressing receive FDA 510(k) clearance?
LUOFUCON Silicone Ag foam dressing received FDA 510(k) clearance on 2016-08-17, under 510(k) number K160022.
Who is the listed applicant for LUOFUCON Silicone Ag foam dressing?
FDA 510(k) 記錄將惠州富友醫療設備有限公司列為申請人。這並不單獨確立設備製造商的身份。
What is the FDA product code for LUOFUCON Silicone Ag foam dressing?
The FDA product code for LUOFUCON Silicone Ag foam dressing is FRO. This falls under the Anesthesiology category.
相關臨床試驗
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。
其他以 Huizhou Foryou Medical Devices 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：FRO）
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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