無液壓計式血壓計；單一病人使用無液壓計式血壓計
K 號：K222652 · 2022-11-28
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器材摘要
常見問題
What is the Aneroid Sphygmomanometer; Single Patient Use Aneroid Sphygmomanometer?
Aneroid Sphygmomanometer; Single Patient Use Aneroid Sphygmomanometer is a medical device that received FDA 510(k) clearance on 2022-11-28. The listed applicant is Cardicare Company, Ltd.. The 510(k) number is K222652.
When did Aneroid Sphygmomanometer; Single Patient Use Aneroid Sphygmomanometer receive FDA 510(k) clearance?
Aneroid Sphygmomanometer; Single Patient Use Aneroid Sphygmomanometer received FDA 510(k) clearance on 2022-11-28, under 510(k) number K222652.
Who is the listed applicant for Aneroid Sphygmomanometer; Single Patient Use Aneroid Sphygmomanometer?
The FDA 510(k) record lists Cardicare Company, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Aneroid Sphygmomanometer; Single Patient Use Aneroid Sphygmomanometer?
The FDA product code for Aneroid Sphygmomanometer; Single Patient Use 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。
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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