FDA 510(k) Applications Submitted by MARY DE ARMOND

FDA 510(k) Number	Submission Date	Device Name	Applicant
K961917	05/17/1996	MEDTRONIC MUSTANG STEERABLE GUIDE WIRE (M-45FR, M45FX)	MEDTRONICS INTERVENTIONAL VASCULAR
K991633	05/12/1999	QUICKVUE INFLUENZA A/B TEST	QUIDEL CORP.
K972944	08/11/1997	MEDTRONIC MUSTANG SUPER FLOPPY GUIDE WIRE/FLOPPY GUIDE WIRE/INTERMEDIATE GUIDE WIRE/STANDARD GUIDE WIRE/EXTRA SUPPORT	MEDTRONICS INTERVENTIONAL VASCULAR