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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Computer, Blood-Pressure
510(k) Number K791838
Device Name HSH/H512 ADULT PHYSIOLOGICAL MONITORS
Applicant
Medtel Pty. , Ltd.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Medtel Pty. , Ltd.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number870.1110
Classification Product Code
DSK  
Date Received09/14/1979
Decision Date 10/01/1979
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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