FDA 510(k)

Electronic Blood Pressure Monitor

K-번호: K200939 · 2020-08-20

신청자Jiangsu Yuyue Medical Equipment & Supply Co., Ltd.

결정일2020-08-20

제품 코드DXN

자문 위원회CV

결정Substantially Equivalent

기기 요약

Electronic Blood Pressure Monitor is the device name listed in this FDA 510(k) record. The listed applicant is Jiangsu Yuyue Medical Equipment & Supply Co., Ltd.. It received FDA 510(k) clearance on 2020-08-20 under 510(k) number K200939. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the Electronic Blood Pressure Monitor?

Electronic Blood Pressure Monitor is a medical device that received FDA 510(k) clearance on 2020-08-20. The listed applicant is Jiangsu Yuyue Medical Equipment & Supply Co., Ltd.. The 510(k) number is K200939.

When did Electronic Blood Pressure Monitor receive FDA 510(k) clearance?

Electronic Blood Pressure Monitor received FDA 510(k) clearance on 2020-08-20, under 510(k) number K200939.

Who is the listed applicant for Electronic Blood Pressure Monitor?

The FDA 510(k) record lists Jiangsu Yuyue Medical Equipment & Supply Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Electronic Blood Pressure Monitor?

The FDA product code for Electronic Blood Pressure Monitor is DXN.

Jiangsu Yuyue Medical Equipment & Supply Co., Ltd.를 신청인으로 등재한 기타 기록

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