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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 K901392
Device Name BP50 BLOOD PRESSURE AND PULSE MONITOR
Applicant
Pulse Time Products, Ltd.
City Gates 2-4 Southgate
Chichester, W. Sussex,  GB PO19 2DJ
Applicant Contact CHATFIELD
Correspondent
Pulse Time Products, Ltd.
City Gates 2-4 Southgate
Chichester, W. Sussex,  GB PO19 2DJ
Correspondent Contact CHATFIELD
Regulation Number870.1130
Classification Product Code
DXN  
Date Received03/26/1990
Decision Date 08/23/1990
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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