Scenium
K 號：K162339 · 2016-09-21
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器材摘要
Scenium is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2016-09-21 under 510(k) number K162339. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Scenium?
Scenium is a medical device that received FDA 510(k) clearance on 2016-09-21. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K162339.
When did Scenium receive FDA 510(k) clearance?
Scenium received FDA 510(k) clearance on 2016-09-21, under 510(k) number K162339.
Who is the listed applicant for Scenium?
The FDA 510(k) record lists Siemens Medical Solutions USA, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Scenium?
The FDA product code for Scenium is LLZ.
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其他以 Siemens Medical Solutions USA, Inc. 為申請人之記錄
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相關器械（代碼：LLZ）
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
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