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FDA 510(k) Applications Submitted by CORDIS EUROPA, N.V.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K060302
02/06/2006
INSCOPE PRECISION BALLOON DILATOR - WIRE GUIDED
CORDIS EUROPA, N.V.
K071189
04/30/2007
CORDIS AVIATOR PLUS PTA BALLOON DILATATION CATHETER
CORDIS EUROPA, N.V.
K043605
12/30/2004
INSCOPE 3-STAGE BALLOON DILATOR
CORDIS EUROPA, N.V.
K063563
11/28/2006
CORDIS AMILA PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY (PTA) BALLOON DILATATION CATHETER
CORDIS EUROPA, N.V.
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