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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Electromyograph, Diagnostic
510(k) Number K864630
Device Name KC/EMG DIAGNOSTIC ELECTROMYOGRAPH
Applicant
Chattanooga Group, Inc.
101 Memorial Dr.
Red Bank,  TN  37405
Applicant Contact BILL CHEAL
Correspondent
Chattanooga Group, Inc.
101 Memorial Dr.
Red Bank,  TN  37405
Correspondent Contact BILL CHEAL
Regulation Number890.1375
Classification Product Code
IKN  
Date Received11/25/1986
Decision Date 12/29/1986
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Physical Medicine
510k Review Panel Neurology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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