PDT-FACE
K 號：K192295 · 2020-05-01
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器材摘要
PDT-FACE is the device name listed in this FDA 510(k) record. The listed applicant is Beijing Adss Development Co., Ltd.. It received FDA 510(k) clearance on 2020-05-01 under 510(k) number K192295. The device is classified under product code OLP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the PDT-FACE?
PDT-FACE is a medical device that received FDA 510(k) clearance on 2020-05-01. The listed applicant is Beijing Adss Development Co., Ltd.. The 510(k) number is K192295.
When did PDT-FACE receive FDA 510(k) clearance?
PDT-FACE received FDA 510(k) clearance on 2020-05-01, under 510(k) number K192295.
Who is the listed applicant for PDT-FACE?
The FDA 510(k) record lists Beijing Adss Development Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PDT-FACE?
The FDA product code for PDT-FACE is OLP.
其他以 Beijing Adss Development Co., Ltd. 為申請人之記錄
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相關器械（代碼：OLP）
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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