FDA 510(k) Application Details - K971307

Device Classification Name	Table, Operating-Room, Ac-Powered   More FDA Info for this Device
510(K) Number	K971307
Device Name	Table, Operating-Room, Ac-Powered
Applicant	STERIS Corporation 5960 HEISLEY RD. MENTOR, OH 44060 US Other 510(k) Applications for this Company
Contact	MATTHEW M HULL 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	04/08/1997
Decision Date	06/27/1997
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review