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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 K900413
Device Name INTELECT 775MP POWERED MUSCLE STIMULATOR
Applicant
Chattanooga Group, Inc.
101 Memorial Dr.
Red Bank,  TN  37405
Applicant Contact GRAHAME WATTS
Correspondent
Chattanooga Group, Inc.
101 Memorial Dr.
Red Bank,  TN  37405
Correspondent Contact GRAHAME WATTS
Regulation Number890.5850
Classification Product Code
IPF  
Date Received01/23/1990
Decision Date 03/07/1990
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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