FDA 510(k) Application Details - K041924

Device Classification Name	Stretcher, Wheeled, Powered   More FDA Info for this Device
510(K) Number	K041924
Device Name	Stretcher, Wheeled, Powered
Applicant	STERIS Corporation 2720 GUNTER PARK DRIVE EAST MONTGOMERY, AL 36101 US Other 510(k) Applications for this Company
Contact	ROBERT H MCCALL 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	07/16/2004
Decision Date	09/09/2004
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