FDA 510(k) Application Details - K991167

Device Classification Name	Apparatus, Exhaust, Surgical   More FDA Info for this Device
510(K) Number	K991167
Device Name	Apparatus, Exhaust, Surgical
Applicant	STERIS Corporation 2720 GUNTER PARK EAST MONTGOMERY, AL 36109 US Other 510(k) Applications for this Company
Contact	ROBERT H MCCALL Other 510(k) Applications for this Contact
Regulation Number	878.5070   More FDA Info for this Regulation Number
Classification Product Code	FYD Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/07/1999
Decision Date	06/03/1999
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Statement
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review