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FDA 510(k)

RH非自動血壓計 RH附聽診器的非自動血壓計

K 號：K190902 · 2019-05-22

申請人Wenzhou Renhua Instruments Co., Ltd.
決定日期2019-05-22
產品代碼DXQ
諮詢委員會履歷
決定相當於

器材摘要

RH non-Automated Blood Pressure Meter RH non-Automated Blood Pressure Meter with Stethoscope is the device name listed in this FDA 510(k) record. The listed applicant is Wenzhou Renhua Instruments Co., Ltd.. It received FDA 510(k) clearance on 2019-05-22 under 510(k) number K190902. 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 RH non-Automated Blood Pressure Meter RH non-Automated Blood Pressure Meter with Stethoscope?

RH non-Automated Blood Pressure Meter RH non-Automated Blood Pressure Meter with Stethoscope is a medical device that received FDA 510(k) clearance on 2019-05-22. The listed applicant is Wenzhou Renhua Instruments Co., Ltd.. The 510(k) number is K190902.

When did RH non-Automated Blood Pressure Meter RH non-Automated Blood Pressure Meter with Stethoscope receive FDA 510(k) clearance?

RH non-Automated Blood Pressure Meter RH non-Automated Blood Pressure Meter with Stethoscope received FDA 510(k) clearance on 2019-05-22, under 510(k) number K190902.

Who is the listed applicant for RH non-Automated Blood Pressure Meter RH non-Automated Blood Pressure Meter with Stethoscope?

The FDA 510(k) record lists Wenzhou Renhua Instruments Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RH non-Automated Blood Pressure Meter RH non-Automated Blood Pressure Meter with Stethoscope?

The FDA product code for RH non-Automated Blood Pressure Meter RH non-Automated Blood Pressure Meter with Stethoscope 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。

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