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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.
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