FDA 510(k)

Scian Automatic Digital Blood Pressure Monitor, Model: LD-576, LD-575 & LD-579

K 號：K170866 · 2018-02-21

決定日期2018-02-21

產品代碼DXN

諮詢委員會履歷

決定相當於

器材摘要

Scian Automatic Digital Blood Pressure Monitor, Model: LD-576, LD-575 & LD-579 is the device name listed in this FDA 510(k) record. The listed applicant is Honsun (Nantong) Co., Ltd.. It received FDA 510(k) clearance on 2018-02-21 under 510(k) number K170866. 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 Scian Automatic Digital Blood Pressure Monitor, Model: LD-576, LD-575 & LD-579?

Scian Automatic Digital Blood Pressure Monitor, Model: LD-576, LD-575 & LD-579 is a medical device that received FDA 510(k) clearance on 2018-02-21. The listed applicant is Honsun (Nantong) Co., Ltd.. The 510(k) number is K170866.

When did Scian Automatic Digital Blood Pressure Monitor, Model: LD-576, LD-575 & LD-579 receive FDA 510(k) clearance?

Scian Automatic Digital Blood Pressure Monitor, Model: LD-576, LD-575 & LD-579 received FDA 510(k) clearance on 2018-02-21, under 510(k) number K170866.

Who is the listed applicant for Scian Automatic Digital Blood Pressure Monitor, Model: LD-576, LD-575 & LD-579?

FDA 510(k) 記錄將宏遠（南通）有限公司列為申請人。這並不單獨確立設備製造商。

What is the FDA product code for Scian Automatic Digital Blood Pressure Monitor, Model: LD-576, LD-575 & LD-579?

The FDA product code for Scian Automatic Digital Blood Pressure Monitor, Model: LD-576, LD-575 & LD-579 is DXN.

其他以 Honsun (Nantong) 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。

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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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