Vascular Architects, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vascular Architects, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Vascular Architects, Inc. has 5 FDA 510(k) cleared medical devices. Based in San Jose, US.
Historical record: 5 cleared submissions from 2001 to 2003. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Vascular Architects, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Vascular Architects, Inc.
5 devices
Cleared
Aug 01, 2003
VASCULAR ARCHITECTS ASPIRE COVERED STENT AND 718 DELIVERY SYSTEM
General & Plastic Surgery
66d
Cleared
Mar 24, 2003
MODIFICATION TO VASCULAR ARCHITECTS ASPIRE COVERED STENT AND CONTRILLED...
General & Plastic Surgery
28d
Cleared
Nov 15, 2001
VASCULAR ARCHITECTS ASPIRE COVERED STENT AND CONTROLLED EXPANSION DELIVERY...
General & Plastic Surgery
100d
Cleared
Mar 13, 2001
ASPIRE COVERED STENT AND DELIVERY CATHETER
Gastroenterology & Urology
154d
Cleared
Feb 28, 2001
VASCULAR ARCHITECTS PERISCOPE DEVICE
Cardiovascular
86d