FDA 510(k) Applications Submitted by Lisa Wells

FDA 510(k) Number	Submission Date	Device Name	Applicant
K971306	04/08/1997	FG INFUSION CATHETER	CORDIS NEUROVASCULAR, INC.
K972518	07/07/1997	TRANSIT/RAPIDTRANSIT/SPEEDSTER/PROWLER INFUSION CATHETER	CORDIS NEUROVASCULAR, INC.
K962765	07/16/1996	CORDIS MARKER WIRE STEERABLE GUIDEWIRE (STABILIZER WITH RADIOPAQUE MARKERS) AND (WIZDOM WITH RADIOPAQUE MARKERS)	CORDIS CORP.
K962932	07/29/1996	CORDIS STABILIZER PLUS XS	CORDIS CORP.
K963171	08/14/1996	CINCH QR SGW EXTENSION	CORDIS CORP.
K963214	08/16/1996	CORDIS ST STEERABLE GUIDEWIRE	CORDIS CORP.
K974222	11/12/1997	CES MASSTRANSIT INFUSION CATHETER	CORDIS NEUROVASCULAR, INC.