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Velocimed, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K052523PROXIS SYSTEMSeptember 7, 2006
K043084PREMERE DELIVERY SHEATH, MODEL PDSMay 2, 2005
K042117PROXIS SYSTEM, MODEL EPS 101January 7, 2005
K042910VENTURE WIRE CONTROL CATHETER, MODEL WCCNovember 22, 2004
K040922VENTURE WIRE CONTROL CATHETERAugust 18, 2004
K023548PROXIS FLOW-CONTROL DEVICE, MODELS EPS 101, IC 101August 4, 2003