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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Stimulator, Nerve, Transcutaneous, For Pain Relief
510(k) Number K920260
Device Name INTELECT 600MP
Applicant
Chattanooga Group, Inc.
4717 Adams Rd.
P.O. Box 4287
Hixson,  TN  37343
Applicant Contact GRAHAME R WATTS
Correspondent
Chattanooga Group, Inc.
4717 Adams Rd.
P.O. Box 4287
Hixson,  TN  37343
Correspondent Contact GRAHAME R WATTS
Regulation Number882.5890
Classification Product Code
GZJ  
Date Received01/21/1992
Decision Date 10/13/1992
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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