Velocimed, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
FDA 510(k) Regulatory Record - Velocimed, Inc. Cardiovascular ✕
5 devices
Cleared
Sep 07, 2006
PROXIS SYSTEM
Cardiovascular
358d
Cleared
May 02, 2005
PREMERE DELIVERY SHEATH, MODEL PDS
Cardiovascular
175d
Cleared
Jan 07, 2005
PROXIS SYSTEM, MODEL EPS 101
Cardiovascular
155d
Cleared
Nov 22, 2004
VENTURE WIRE CONTROL CATHETER, MODEL WCC
Cardiovascular
32d
Cleared
Aug 18, 2004
VENTURE WIRE CONTROL CATHETER
Cardiovascular
132d