內部交換式潛葉
K 號：K203231 · 2021-01-11
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器材摘要
Switched Internal Paddles is the device name listed in this FDA 510(k) record. The listed applicant is Philips North America, LLC. It received FDA 510(k) clearance on 2021-01-11 under 510(k) number K203231. The device is classified under product code LDD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Switched Internal Paddles?
Switched Internal Paddles is a medical device that received FDA 510(k) clearance on 2021-01-11. The listed applicant is Philips North America, LLC. The 510(k) number is K203231.
When did Switched Internal Paddles receive FDA 510(k) clearance?
Switched Internal Paddles received FDA 510(k) clearance on 2021-01-11, under 510(k) number K203231.
Who is the listed applicant for Switched Internal Paddles?
The FDA 510(k) record lists Philips North America, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Switched Internal Paddles?
The FDA product code for Switched Internal Paddles is LDD.
相關臨床試驗
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相關器械（代碼：LDD）
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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