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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Table, Mechanical
510(k) Number K801643
Device Name TRITON
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 Number890.3750
Classification Product Code
INW  
Date Received07/17/1980
Decision Date 07/28/1980
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
Recalls CDRH Recalls
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