Vnus Medical Technologies, Inc. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
FDA 510(k) Regulatory Record - Vnus Medical Technologies, Inc. General & Plastic Surgery ✕
9 devices
Cleared
Oct 15, 2008
VNUS CLOSUREFAST INTRAVASCULAR CATHETER, MODELS CF7-7-60-2, CF7-7-100-2
General & Plastic Surgery
15d
Cleared
Aug 01, 2006
VNUS CLOSUREFAST CATHETER, MODELS CF7-7-60 AND CF7-7-100
General & Plastic Surgery
76d
Cleared
Oct 11, 2005
VNUS RFS, MODEL RFS-6-XX (XX = 10, 12, 13, & 15)
General & Plastic Surgery
78d
Cleared
Jun 07, 2004
VNUS RADIOFREQUENCY GENERATOR, MODEL RFG2
General & Plastic Surgery
89d
Cleared
Jan 07, 2004
VNUS VESSEL AND TISSUE COAGULATION SYSTEM
General & Plastic Surgery
56d
Cleared
Mar 11, 2003
MODIFICATION TO VNUS CLOSURE SYSTEM
General & Plastic Surgery
18d
Cleared
Dec 18, 2000
MODIFICATION TO VNUS CLOSURE SYSTEM
General & Plastic Surgery
76d
Cleared
Mar 17, 1999
VNUS CLOSURE SYSTEM
General & Plastic Surgery
218d
Cleared
Feb 20, 1998
VNUS CLOSURE SYSTEM
General & Plastic Surgery
80d