Seca醫療生命徵象分析儀535，Seca mVSA 535，Seca mVSA，Seca 535
K 號：K192092 · 2020-01-23
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器材摘要
常見問題
What is the Seca Medical Vital Signs Analyzer 535, Seca mVSA 535, Seca mVSA, Seca 535?
Seca Medical Vital Signs Analyzer 535, Seca mVSA 535, Seca mVSA, Seca 535 is a medical device that received FDA 510(k) clearance on 2020-01-23. The listed applicant is Seca GmbH & Co. KG. The 510(k) number is K192092.
When did Seca Medical Vital Signs Analyzer 535, Seca mVSA 535, Seca mVSA, Seca 535 receive FDA 510(k) clearance?
Seca Medical Vital Signs Analyzer 535, Seca mVSA 535, Seca mVSA, Seca 535 received FDA 510(k) clearance on 2020-01-23, under 510(k) number K192092.
Who is the listed applicant for Seca Medical Vital Signs Analyzer 535, Seca mVSA 535, Seca mVSA, Seca 535?
The FDA 510(k) record lists Seca GmbH & Co. KG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Seca Medical Vital Signs Analyzer 535, Seca mVSA 535, Seca mVSA, Seca 535?
The FDA product code for Seca Medical Vital Signs Analyzer 535, Seca mVSA 535, Seca mVSA, Seca 535 is DXN.
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相關器械（代碼：DXN）
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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