FDA 510(k) Application Details - K090136

Device Classification Name	Table, Operating-Room, Ac-Powered   More FDA Info for this Device
510(K) Number	K090136
Device Name	Table, Operating-Room, Ac-Powered
Applicant	STERIS Corporation 5960 Heisley Road Mentor, OH 44060 US Other 510(k) Applications for this Company
Contact	JOHN ROBERT SCOVILLE Other 510(k) Applications for this Contact
Regulation Number	878.4960   More FDA Info for this Regulation Number
Classification Product Code	FQO Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/21/2009
Decision Date	03/20/2009
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review