Vnus Medical Technologies, Inc.
FDA 510(k) & PMA Approved Devices — 9 products
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Total Devices9
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K082890 | VNUS CLOSUREFAST INTRAVASCULAR CATHETER, MODELS CF7-7-60-2, CF7-7-100-2 | GEI | 2008-10-15 | View |
| 510(k) | K061373 | VNUS CLOSUREFAST CATHETER, MODELS CF7-7-60 AND CF7-7-100 | GEI | 2006-08-01 | View |
| 510(k) | K052003 | VNUS RFS, MODEL RFS-6-XX (XX = 10, 12, 13, & 15); VNUS RFS FLEX, MODEL RFX-6-XX (XX = 10, 20, 30 & 40) | GEI | 2005-10-11 | View |
| 510(k) | K040638 | VNUS RADIOFREQUENCY GENERATOR, MODEL RFG2 | GEI | 2004-06-07 | View |
| 510(k) | K033547 | VNUS VESSEL AND TISSUE COAGULATION SYSTEM | GEI | 2004-01-07 | View |
| 510(k) | K030557 | MODIFICATION TO VNUS CLOSURE SYSTEM | GEI | 2003-03-11 | View |
| 510(k) | K003092 | MODIFICATION TO VNUS CLOSURE SYSTEM | GEI | 2000-12-18 | View |
| 510(k) | K982816 | VNUS CLOSURE SYSTEM | GEI | 1999-03-17 | View |
| 510(k) | K974521 | VNUS CLOSURE SYSTEM | GEI | 1998-02-20 | View |
No matching devices.
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