FDA 510(k)

血壓監測器-型號 2005, 2006-2, 2006-2B

K 號：K201467 · 2020-09-21

決定日期2020-09-21

產品代碼DXN

諮詢委員會履歷

決定相當於

器材摘要

Blood Pressure Monitor-Model 2005, 2006-2, 2006-2B is the device name listed in this FDA 510(k) record. The listed applicant is Bioland Technology, Ltd.. It received FDA 510(k) clearance on 2020-09-21 under 510(k) number K201467. 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 Blood Pressure Monitor-Model 2005, 2006-2, 2006-2B?

Blood Pressure Monitor-Model 2005, 2006-2, 2006-2B is a medical device that received FDA 510(k) clearance on 2020-09-21. The listed applicant is Bioland Technology, Ltd.. The 510(k) number is K201467.

When did Blood Pressure Monitor-Model 2005, 2006-2, 2006-2B receive FDA 510(k) clearance?

Blood Pressure Monitor-Model 2005, 2006-2, 2006-2B received FDA 510(k) clearance on 2020-09-21, under 510(k) number K201467.

Who is the listed applicant for Blood Pressure Monitor-Model 2005, 2006-2, 2006-2B?

The FDA 510(k) record lists Bioland Technology, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Blood Pressure Monitor-Model 2005, 2006-2, 2006-2B?

The FDA product code for Blood Pressure Monitor-Model 2005, 2006-2, 2006-2B is DXN.

其他以 Bioland Technology, 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。

K202739Bioland G-425-2V 血糖監測系統，Bioland G-425-2 血糖監測系統 K213011紅外線體溫計（型號：E201）K201879數位體溫計模型 T103, T104 K202934血壓監測器 K201161紅外線體溫計模型 E127 K191657Bioland 血糖監測系統

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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。

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