無液壓計式血壓計
K 號：K203620 · 2021-03-23
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器材摘要
Aneroid Sphygmomanometer is the device name listed in this FDA 510(k) record. The listed applicant is Wuxi Exanovo Medical Instrument Co., Ltd.. It received FDA 510(k) clearance on 2021-03-23 under 510(k) number K203620. The device is classified under product code DXQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Aneroid Sphygmomanometer?
Aneroid Sphygmomanometer is a medical device that received FDA 510(k) clearance on 2021-03-23. The listed applicant is Wuxi Exanovo Medical Instrument Co., Ltd.. The 510(k) number is K203620.
When did Aneroid Sphygmomanometer receive FDA 510(k) clearance?
Aneroid Sphygmomanometer received FDA 510(k) clearance on 2021-03-23, under 510(k) number K203620.
Who is the listed applicant for Aneroid Sphygmomanometer?
The FDA 510(k) record lists Wuxi Exanovo Medical Instrument Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Aneroid Sphygmomanometer?
The FDA product code for Aneroid Sphygmomanometer is DXQ.
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相關器械（代碼：DXQ）
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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