FDA 510(k) Applications Submitted by JOAN MARTIN

FDA 510(k) Number	Submission Date	Device Name	Applicant
K980823	03/03/1998	CORDIS NITINOL STENT AND DELIVERY SYSTEM	CORDIS CORP.
K101651	06/11/2010	ANGIOGUARD XP EMBOLI CAPTURE GUIDEWIRE, ANGIOGUARD RX EMBOLI CAPTURE GUIDEWIRE	CORDIS CORP.
K062531	08/29/2006	ANGIOGUARD XP EMBOLI CAPTURE GUIDEWIRE AND ANGIOGUARD RX EMBOLI CAPTURE GUIDEWIRE	CORDIS CORP., A JOHNSON & JOHNSON CO.
K964688	11/22/1996	LONG MEDIUM PALMAZ-SCHATZ BALLOON EXPANDABLE STENT	CORDIS CORP.
K063563	11/28/2006	CORDIS AMILA PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY (PTA) BALLOON DILATATION CATHETER	CORDIS EUROPA, N.V.