FDA 510(k)

可重用血壓袖帶

K 號：K171889 · 2017-12-19

申請人Suzhou Minhua Medical Apparatus Supplies Co., Ltd.

決定日期2017-12-19

產品代碼DXQ

諮詢委員會履歷

決定相當於

器材摘要

Reusable Blood Pressure Cuff is the device name listed in this FDA 510(k) record. The listed applicant is Suzhou Minhua Medical Apparatus Supplies Co., Ltd.. It received FDA 510(k) clearance on 2017-12-19 under 510(k) number K171889. 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 Reusable Blood Pressure Cuff?

Reusable Blood Pressure Cuff is a medical device that received FDA 510(k) clearance on 2017-12-19. The listed applicant is Suzhou Minhua Medical Apparatus Supplies Co., Ltd.. The 510(k) number is K171889.

When did Reusable Blood Pressure Cuff receive FDA 510(k) clearance?

Reusable Blood Pressure Cuff received FDA 510(k) clearance on 2017-12-19, under 510(k) number K171889.

Who is the listed applicant for Reusable Blood Pressure Cuff?

The FDA 510(k) record lists Suzhou Minhua Medical Apparatus Supplies Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Reusable Blood Pressure Cuff?

The FDA product code for Reusable Blood Pressure Cuff is DXQ.

其他以 Suzhou Minhua Medical Apparatus Supplies 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：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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