皮茲頓內置套件，皮茲頓內置套件LED
K 號：K191079 · 2019-08-16
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器材摘要
常見問題
What is the Piezon Built-in Kit, Piezon Built-in Kit LED?
Piezon Built-in Kit, Piezon Built-in Kit LED is a medical device that received FDA 510(k) clearance on 2019-08-16. The listed applicant is E.M.S Electro Medical Systems S.A. The 510(k) number is K191079.
When did Piezon Built-in Kit, Piezon Built-in Kit LED receive FDA 510(k) clearance?
Piezon Built-in Kit, Piezon Built-in Kit LED received FDA 510(k) clearance on 2019-08-16, under 510(k) number K191079.
Who is the listed applicant for Piezon Built-in Kit, Piezon Built-in Kit LED?
The FDA 510(k) record lists E.M.S Electro Medical Systems S.A as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Piezon Built-in Kit, Piezon Built-in Kit LED?
The FDA product code for Piezon Built-in Kit, Piezon Built-in Kit LED is ELC.
相關臨床試驗
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其他以 E.M.S Electro Medical Systems S.A 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：ELC）
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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