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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 K832075
Device Name ELECTRONIC BLOOD PRESS. METER-ZH-820P
Applicant
Panasonic Co. Div. Matsu Elec. Corp. America
.
Nutley,  NJ 
Correspondent
Panasonic Co. Div. Matsu Elec. Corp. America
.
Nutley,  NJ 
Regulation Number870.1130
Classification Product Code
DXN  
Date Received06/28/1983
Decision Date 08/12/1983
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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