FDA 510(k) Application Details - K962168

Device Classification Name	Bottle, Collection, Vacuum   More FDA Info for this Device
510(K) Number	K962168
Device Name	Bottle, Collection, Vacuum
Applicant	SAGE PRODUCTS, INC. 815 TEK DR. CRYSTAL LAKE, IL 60014-8172 US Other 510(k) Applications for this Company
Contact	KAREN PINTO Other 510(k) Applications for this Contact
Regulation Number	880.6740   More FDA Info for this Regulation Number
Classification Product Code	KDQ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/05/1996
Decision Date	07/22/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review