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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Table, Powered
510(k) Number K960196
Device Name TRI W-G, INC TABLE, TILT/EXAM/TREATMENT MODEL 777
Applicant
Tri W-G, Inc.
215 12th Ave., NE
P.O. Box 905
Valley City,  ND  58072
Applicant Contact DAVID KESLER
Correspondent
Tri W-G, Inc.
215 12th Ave., NE
P.O. Box 905
Valley City,  ND  58072
Correspondent Contact DAVID KESLER
Regulation Number890.3760
Classification Product Code
INQ  
Date Received01/16/1996
Decision Date 02/07/1996
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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