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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Wheelchair, Mechanical
510(k) Number K023606
Device Name TILITE YG AND TILITE YGS
Applicant
Tisport
1426 E. Third Ave.
Kennewick,  WA  99337 -9669
Applicant Contact RICHARD S FORMAN
Correspondent
Tisport
1426 E. Third Ave.
Kennewick,  WA  99337 -9669
Correspondent Contact RICHARD S FORMAN
Regulation Number890.3850
Classification Product Code
IOR  
Date Received10/28/2002
Decision Date 11/19/2002
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Physical Medicine
510k Review Panel Physical Medicine
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
Recalls CDRH Recalls
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