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U.S. Department of Health and Human Services

510(k) Premarket Notification
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510(k) Number K904722
Device Name FLUOROSCOPIC TABLE, TILT OR POWER TILTING MED. TAB
Applicant
Tri W-G, Inc.
P.O. Box 905
Valley City,  ND  58072
Applicant Contact DAVID KESLER
Correspondent
Tri W-G, Inc.
P.O. Box 905
Valley City,  ND  58072
Correspondent Contact DAVID KESLER
Date Received10/18/1990
Decision Date 01/23/1991
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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