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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Stretcher, Wheeled, Powered
510(k) Number K022309
Device Name STRYKER POWERED WHEELED STRETCHER
Applicant
Stryker Corp.
1730 Pennsylvania Ave. NW
Washington,  DC  20006 -4706
Applicant Contact LYNETTE GABRIEL
Correspondent
Stryker Corp.
1730 Pennsylvania Ave. NW
Washington,  DC  20006 -4706
Correspondent Contact LYNETTE GABRIEL
Regulation Number890.3690
Classification Product Code
INK  
Date Received07/16/2002
Decision Date 11/08/2002
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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