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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name System, Measurement, Blood-Pressure, Non-Invasive
510(k) Number K200521
Device Name Full Automatic(NIBP) Blood Pressure Monitor
Applicant
Health & Life Co., Ltd.
9f, # 186 Jian Yi Rd.,
Zhonghe District, New Taipei City,  TW 23553
Applicant Contact Simon Lee
Correspondent
Health & Life Co., Ltd.
9f, # 186 Jian Yi Rd.,
Zhonghe District, New Taipei City,  TW 23553
Correspondent Contact Simon Lee
Regulation Number870.1130
Classification Product Code
DXN  
Date Received03/02/2020
Decision Date 06/12/2020
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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