ASI 肺活量測定儀
K 號：K200567 · 2021-02-26
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器材摘要
ASI Plethysmogrpah Analyzer is the device name listed in this FDA 510(k) record. The listed applicant is Arterial Stiffness, Inc.. It received FDA 510(k) clearance on 2021-02-26 under 510(k) number K200567. The device is classified under product code JOM. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the ASI Plethysmogrpah Analyzer?
ASI Plethysmogrpah Analyzer is a medical device that received FDA 510(k) clearance on 2021-02-26. The listed applicant is Arterial Stiffness, Inc.. The 510(k) number is K200567.
When did ASI Plethysmogrpah Analyzer receive FDA 510(k) clearance?
ASI Plethysmogrpah Analyzer received FDA 510(k) clearance on 2021-02-26, under 510(k) number K200567.
Who is the listed applicant for ASI Plethysmogrpah Analyzer?
The FDA 510(k) record lists Arterial Stiffness, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ASI Plethysmogrpah Analyzer?
The FDA product code for ASI Plethysmogrpah Analyzer is JOM.
相關臨床試驗
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相關器械（代碼：JOM）
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
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