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FDA 510(k)

AGE自動上臂血壓監測儀,型號BA-815, BA-816, BA-818和BA-819

K 號:K172895 · 2018-06-18

決定日期2018-06-18
產品代碼DXN
諮詢委員會履歷
決定相當於

器材摘要

AGE Automatic Upper Arm Blood Pressure Monitor with models BA-815, BA-816, BA-818 and BA-819 is the device name listed in this FDA 510(k) record. The listed applicant is Ageless Health Industrial Co., Ltd.. It received FDA 510(k) clearance on 2018-06-18 under 510(k) number K172895. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the AGE Automatic Upper Arm Blood Pressure Monitor with models BA-815, BA-816, BA-818 and BA-819?

AGE Automatic Upper Arm Blood Pressure Monitor with models BA-815, BA-816, BA-818 and BA-819 is a medical device that received FDA 510(k) clearance on 2018-06-18. The listed applicant is Ageless Health Industrial Co., Ltd.. The 510(k) number is K172895.

When did AGE Automatic Upper Arm Blood Pressure Monitor with models BA-815, BA-816, BA-818 and BA-819 receive FDA 510(k) clearance?

AGE Automatic Upper Arm Blood Pressure Monitor with models BA-815, BA-816, BA-818 and BA-819 received FDA 510(k) clearance on 2018-06-18, under 510(k) number K172895.

Who is the listed applicant for AGE Automatic Upper Arm Blood Pressure Monitor with models BA-815, BA-816, BA-818 and BA-819?

The FDA 510(k) record lists Ageless Health Industrial Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AGE Automatic Upper Arm Blood Pressure Monitor with models BA-815, BA-816, BA-818 and BA-819?

The FDA product code for AGE Automatic Upper Arm Blood Pressure Monitor with models BA-815, BA-816, BA-818 and BA-819 is DXN.

相關臨床試驗

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。

其他以 Ageless Health Industrial Co., Ltd. 為申請人之記錄

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。

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

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