CPM系統
K 號：K231086 · 2023-12-22
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器材摘要
CPM System is the device name listed in this FDA 510(k) record. The listed applicant is Analog Devices, Inc.. It received FDA 510(k) clearance on 2023-12-22 under 510(k) number K231086. The device is classified under product code MWI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the CPM System?
CPM System is a medical device that received FDA 510(k) clearance on 2023-12-22. The listed applicant is Analog Devices, Inc.. The 510(k) number is K231086.
When did CPM System receive FDA 510(k) clearance?
CPM System received FDA 510(k) clearance on 2023-12-22, under 510(k) number K231086.
Who is the listed applicant for CPM System?
The FDA 510(k) record lists Analog Devices, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CPM System?
The FDA product code for CPM System is MWI.
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相關器械（代碼：MWI）
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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