Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Vnus Medical Technologies, Inc. · Predicate Candidate Screening
9 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
76 daysmedian FDA review time
218 days90th percentile
9clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K082890 | VNUS CLOSUREFAST INTRAVASCULAR CATHETER, MODELS CF7-7-60-2, | Vnus Medical Technologies, Inc. | 2008-10-15 | 15 | 0 |
| K061373 | VNUS CLOSUREFAST CATHETER, MODELS CF7-7-60 AND CF7-7-100 | Vnus Medical Technologies, Inc. | 2006-08-01 | 76 | 2 |
| K052003 | VNUS RFS, MODEL RFS-6-XX (XX = 10, 12, 13, & 15); VNUS RFS F | Vnus Medical Technologies, Inc. | 2005-10-11 | 78 | 0 |
| K040638 | VNUS RADIOFREQUENCY GENERATOR, MODEL RFG2 | Vnus Medical Technologies, Inc. | 2004-06-07 | 89 | 0 |
| K033547 | VNUS VESSEL AND TISSUE COAGULATION SYSTEM | Vnus Medical Technologies, Inc. | 2004-01-07 | 56 | 0 |
| K030557 | MODIFICATION TO VNUS CLOSURE SYSTEM | Vnus Medical Technologies, Inc. | 2003-03-11 | 18 | 0 |
| K003092 | MODIFICATION TO VNUS CLOSURE SYSTEM | Vnus Medical Technologies, Inc. | 2000-12-18 | 76 | 0 |
| K982816 | VNUS CLOSURE SYSTEM | Vnus Medical Technologies, Inc. | 1999-03-17 | 218 | 0 |
| K974521 | VNUS CLOSURE SYSTEM | Vnus Medical Technologies, Inc. | 1998-02-20 | 80 | 0 |
Methodology
Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.
Prepared with Atlas
Predicate research, review-time statistics and recall monitoring for 510(k) teams: atlasbyauro.com/fda