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FDA 510(k) Applications Submitted by VASCULAR ARCHITECTS, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K012544
08/07/2001
VASCULAR ARCHITECTS ASPIRE COVERED STENT AND CONTROLLED EXPANSION DELIVERY SYSTEM
VASCULAR ARCHITECTS, INC.
K003719
12/04/2000
VASCULAR ARCHITECTS PERISCOPE DEVICE
VASCULAR ARCHITECTS, INC.
K003173
10/10/2000
ASPIRE COVERED STENT AND DELIVERY CATHETER
VASCULAR ARCHITECTS, INC.
K030567
02/24/2003
MODIFICATION TO VASCULAR ARCHITECTS ASPIRE COVERED STENT AND CONTRILLED EXPANSION DELIVERY SYSTEM
VASCULAR ARCHITECTS, INC.
K031641
05/27/2003
VASCULAR ARCHITECTS ASPIRE COVERED STENT AND 718 DELIVERY SYSTEM
VASCULAR ARCHITECTS, INC.
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