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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