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U.S. Department of Health and Human Services

510(k) Premarket Notification
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510(k) Number K827034
Device Name INTELECT MODEL 200
Applicant
Chattanooga Group, Inc.
4717 Adams Rd.
P.O. Box 4287
Hixson,  TN  37343
Correspondent
Chattanooga Group, Inc.
4717 Adams Rd.
P.O. Box 4287
Hixson,  TN  37343
Date Received01/05/1982
Decision Date 02/22/1982
Decision Substantially Equivalent (SESE)
510k Review Panel Radiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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