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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Bed, Patient Rotation, Powered
510(k) Number K810220
Device Name POWERED PATIENT SYSTEM
Applicant
Tri W-G, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Tri W-G, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number890.5225
Classification Product Code
IKZ  
Date Received01/27/1981
Decision Date 02/04/1981
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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