FDA 510(k) Application Details - K031339

Device Classification Name	Injector And Syringe, Angiographic   More FDA Info for this Device
510(K) Number	K031339
Device Name	Injector And Syringe, Angiographic
Applicant	MALLINCKRODT INC., LIEBEL-FLARSHEIM BUSINESS 2111 EAST GALBRAITH RD. CINCINNATI, OH 45237 US Other 510(k) Applications for this Company
Contact	ELLIS ROGERS Other 510(k) Applications for this Contact
Regulation Number	870.1650   More FDA Info for this Regulation Number
Classification Product Code	DXT Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/28/2003
Decision Date	07/11/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review