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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 K864411
Device Name PULSE/B.P. MONITOR
Applicant
PULSE TIME PRODUCTS, LTD.
CITY GATES 2-4 SOUTHGATE
CHICHESTER, W. SUSSEX,  GB PO19 2DJ
Applicant Contact LEVESLEY
Correspondent
PULSE TIME PRODUCTS, LTD.
CITY GATES 2-4 SOUTHGATE
CHICHESTER, W. SUSSEX,  GB PO19 2DJ
Correspondent Contact LEVESLEY
Regulation Number870.1130
Classification Product Code
DXN  
Date Received11/07/1986
Decision Date 06/24/1987
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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