ClearanceBrief
Company ยท US

Vascular Architects, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2001 to 2003. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
JCTProsthesis, Tracheal, Expandable3
DWXStripper, Artery, Intraluminal1
ESWProsthesis, Esophageal1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Aug 1, 2003K031641VASCULAR ARCHITECTS ASPIRE COVERED STENT AND 718 DELIVERY SYSTEM
Vascular Architects, Inc.
JCT
Mar 24, 2003K030567MODIFICATION TO VASCULAR ARCHITECTS ASPIRE COVERED STENT AND CONTRILLED EXPANSION DELIVERY SYSTEM
Vascular Architects, Inc.
JCT
Nov 15, 2001K012544VASCULAR ARCHITECTS ASPIRE COVERED STENT AND CONTROLLED EXPANSION DELIVERY SYSTEM
Vascular Architects, Inc.
JCT
Mar 13, 2001K003173ASPIRE COVERED STENT AND DELIVERY CATHETER
Vascular Architects, Inc.
ESW
Feb 28, 2001K003719VASCULAR ARCHITECTS PERISCOPE DEVICE
Vascular Architects, Inc.
DWX

Latest recalls

DateFirm and productCodeLinked 510(k)
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