FDA 510(k) Application Details - K022309

Device Classification Name	Stretcher, Wheeled, Powered   More FDA Info for this Device
510(K) Number	K022309
Device Name	Stretcher, Wheeled, Powered
Applicant	STRYKER CORP. 1730 PENNSYLVANIA AVENUE N.W. WASHINGTON, DC 20006-4706 US Other 510(k) Applications for this Company
Contact	LYNETTE GABRIEL Other 510(k) Applications for this Contact
Regulation Number	890.3690   More FDA Info for this Regulation Number
Classification Product Code	INK Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/16/2002
Decision Date	11/08/2002
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	PM - Physical Medicine
Review Advisory Committee	PM - Physical Medicine
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review