FDA 510(k) Application Details - K960581

Device Classification Name	Container, I.V.   More FDA Info for this Device
510(K) Number	K960581
Device Name	Container, I.V.
Applicant	SECURE MEDICAL PRODUCTS, INC. 369 N. NEWCOMB ST. WHITEWATER, WI 53190 US Other 510(k) Applications for this Company
Contact	LISA M BECK Other 510(k) Applications for this Contact
Regulation Number	880.5025   More FDA Info for this Regulation Number
Classification Product Code	KPE Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/12/1996
Decision Date	04/30/1996
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