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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Stimulator, Muscle, Powered
510(k) Number K801790
Device Name INTELECT
Applicant
CHATTANOOGA GROUP, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
CHATTANOOGA GROUP, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number890.5850
Classification Product Code
IPF  
Date Received07/29/1980
Decision Date 08/20/1980
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Physical Medicine
510k Review Panel Physical Medicine
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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