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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Blood Pressure Cuff
510(k) Number K821232
Device Name ONE HAND ANEROID SPHYGMOMANOMETER
Applicant
ABCO DEALERS, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
ABCO DEALERS, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number870.1120
Classification Product Code
DXQ  
Date Received04/28/1982
Decision Date 05/25/1982
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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