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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