MOBILETT 震擊
K 號：K231577 · 2023-07-25
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器材摘要
MOBILETT Impact is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Solutions. It received FDA 510(k) clearance on 2023-07-25 under 510(k) number K231577. The device is classified under product code IZL. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the MOBILETT Impact?
MOBILETT Impact is a medical device that received FDA 510(k) clearance on 2023-07-25. The listed applicant is Siemens Medical Solutions. The 510(k) number is K231577.
When did MOBILETT Impact receive FDA 510(k) clearance?
MOBILETT Impact received FDA 510(k) clearance on 2023-07-25, under 510(k) number K231577.
Who is the listed applicant for MOBILETT Impact?
The FDA 510(k) record lists Siemens Medical Solutions as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MOBILETT Impact?
The FDA product code for MOBILETT Impact is IZL.
相關臨床試驗
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其他以 Siemens Medical Solutions 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：IZL）
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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