E>眼視設備 FDA 510(k) PMA NCT PMID 識別碼 網址
K 號:K200616 · 2020-06-11
廣告
器材摘要
E>EyeC is the device name listed in this FDA 510(k) record. The listed applicant is E-Swin. It received FDA 510(k) clearance on 2020-06-11 under 510(k) number K200616. The device is classified under product code ONF. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the E>EyeC?
E>EyeC is a medical device that received FDA 510(k) clearance on 2020-06-11. The listed applicant is E-Swin. The 510(k) number is K200616.
When did E>EyeC receive FDA 510(k) clearance?
E>EyeC received FDA 510(k) clearance on 2020-06-11, under 510(k) number K200616.
Who is the listed applicant for E>EyeC?
The FDA 510(k) record lists E-Swin as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for E>EyeC?
The FDA product code for E>EyeC is ONF.
相關器械(代碼:ONF)
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。
K261204強烈脈衝光療法設備Sanhe LEFIS Electronics Co., Ltd.K251545強烈脈衝光療法設備(MMABM-1)Micowey Medical Equipment (Guangxi) Co., Ltd.K231952醫療設備名稱:MEDILIGHTMedicreations, LLCK243123IPL治療設備(MDSQMC-01)Medusa (Guangxi)Medical Devices Co., Ltd.K250281DEKA 草莓El.En S.P.A.K242440強烈脈衝光治療系統(LK-PT)Nanjing Bestview Laser S&T Co., Ltd.
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。
廣告