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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 K942488
Device Name MEDCUFF
Applicant
Med-Con, Inc.
P.O. Box 490
Townsend,  TN  37882
Applicant Contact H. CLAY WILSON
Correspondent
Med-Con, Inc.
P.O. Box 490
Townsend,  TN  37882
Correspondent Contact H. CLAY WILSON
Regulation Number870.1120
Classification Product Code
DXQ  
Date Received05/25/1994
Decision Date 08/23/1994
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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