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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 AVENUE N.W.
WASHINGTON,  DC  20006 -4706
Applicant Contact LYNETTE GABRIEL
Correspondent
STRYKER CORP.
1730 PENNSYLVANIA AVENUE N.W.
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
Recalls CDRH Recalls
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