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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Recorder, Magnetic Tape, Medical
510(k) Number K771932
Device Name RECORDER, DINMAP, MODEL 950
Applicant
APPLIED MEDICAL RESEARCH
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
APPLIED MEDICAL RESEARCH
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number870.2800
Classification Product Code
DSH  
Date Received10/14/1977
Decision Date 11/07/1977
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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