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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 K170467
Device Name Microlife Upper Arm Automatic Digital Blood Pressure Monitor
Microlife Intellectual Property GmbH
Espenstrasse 139
widnau,  CH 9443
Applicant Contact gerhard frick
mdi Consultant, Inc.
55 Northem Blvd.
great neck,  NY  11021
Correspondent Contact susan d. goldstein-falk
Regulation Number870.1130
Classification Product Code
Date Received02/16/2017
Decision Date 08/30/2017
Decision substantially equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Type Traditional
Reviewed by Third Party No
Combination Product No