名照明探針搭配切換器
K 號：K202670 · 2021-08-20
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器材摘要
Nam illumination probe with chopper is the device name listed in this FDA 510(k) record. The listed applicant is Oculight , Ltd.. It received FDA 510(k) clearance on 2021-08-20 under 510(k) number K202670. The device is classified under product code MPA. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Nam illumination probe with chopper?
Nam illumination probe with chopper is a medical device that received FDA 510(k) clearance on 2021-08-20. The listed applicant is Oculight , Ltd.. The 510(k) number is K202670.
When did Nam illumination probe with chopper receive FDA 510(k) clearance?
Nam illumination probe with chopper received FDA 510(k) clearance on 2021-08-20, under 510(k) number K202670.
Who is the listed applicant for Nam illumination probe with chopper?
The FDA 510(k) record lists Oculight , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Nam illumination probe with chopper?
The FDA product code for Nam illumination probe with chopper is MPA.
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。
相關器械（代碼：MPA）
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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