多利克衝擊E
K 號：K233532 · 2023-11-29
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器材摘要
MULTIX Impact E 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 2023-11-29 under 510(k) number K233532. The device is classified under product code KPR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the MULTIX Impact E?
MULTIX Impact E is a medical device that received FDA 510(k) clearance on 2023-11-29. The listed applicant is Siemens Medical Solutions. The 510(k) number is K233532.
When did MULTIX Impact E receive FDA 510(k) clearance?
MULTIX Impact E received FDA 510(k) clearance on 2023-11-29, under 510(k) number K233532.
Who is the listed applicant for MULTIX Impact E?
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 MULTIX Impact E?
The FDA product code for MULTIX Impact E is KPR.
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：KPR）
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。
K260227EXSYS DEXi (EXSYS DEXi-S40S)；EXSYS DEXi (EXSYS DEXi-S40P)；EXSYS DEXi (EXSYS DEXi-S40T)；EXSYS DEXi (EXSYS DEXi-S50H)DRTECH CorporationK260488MULTIX 震擊；MULTIX 震擊 CSiemens Medical Solutions USA, Inc.K260481GC85ASamsung Electronics Co., Ltd.K260482DRE 雙用設備Jpi Healthcare Co, Ltd.K253446AeroDR TX c02Dk Medical Systems Co., Ltd.K250954DRX-Evolution Plus 電影系統，DRX-Compass 流動電影系統，Lux HD 35 探測器，Lux HD 43 探測器Carestream Health
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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