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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Densitometer
510(k) Number K791892
Device Name TAPE-A-TRACE
Applicant
INSTROMEDIX, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
INSTROMEDIX, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number870.1450
Classification Product Code
DXM  
Date Received09/25/1979
Decision Date 11/05/1979
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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