510(k) · Cleared
ClearedClosurefast Radiofrequency Catheter
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Covidien · GEI Electrosurgical, Cutting & Coagulation & Accessories
Cleared on Sep 9, 2011 as substantially equivalent to K061373 (Vnus Medical Technologies, Inc., 2006) after a 70-day review. Its family tree reaches back 9 generations to 1995. 6 later devices descend from it.
- Decided
- Sep 9, 2011
- Review
- 70 days
- Class
- Class II
- Product code
- GEI
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 9 generations to K943450 (1995). 24 ancestors in all, the oldest K800617 (1980). 6 later devices descend from it, 6 citing it directly.
- Root · 9 generations backK943450 Arthrocare Arthroscopic Electrosurgery System Model 970Arthrocare Corp. · 1995
- 5 generations between
- 3 generations backK982816 Vnus Closure SystemVnus Medical Technologies, Inc. · 1999
- 2 generations backK030557 Modification to Vnus Closure SystemVnus Medical Technologies, Inc. · 2003
- 1 generation backK061373 Vnus Closurefast Catheter, Models CF7-7-60 and CF7-7-100Vnus Medical Technologies, Inc. · 2006 · Recalled
- This deviceK111887 Closurefast Radiofrequency CatheterCovidien · 2011
- Descendant · cites it directly · 0 of its ownK253918 Veineo System (00MEDRF4000TCUS 05CR45iT 06Pedal1St)F Care Systems USA, LLC · 2026
- Descendant · cites it directly · 0 of its ownK250688 Cedar™ Endovenous Radiofrequency Catheter (ERA-C70-US); Cedar™…Acotec Scientific Co., Ltd. · 2025
- Descendant · cites it directly · 0 of its ownK222997 VVR Generator systemStarmed Co., Ltd. · 2023
- Descendant · cites it directly · 0 of its ownK223488 ClosureFast™ Endovenous Radiofrequency Ablation CatheterMedtronic, Inc. · 2023
- Descendant · cites it directly · 0 of its ownK191073 Vein360 Endovenous Radiofrequency Ablation (RFA) CatheterVein 360, LLC · 2019
Show all 9 generations
- Root · 9 generations backK943450 Arthrocare Arthroscopic Electrosurgery System Model 970Arthrocare Corp. · 1995
- 8 generations backK961069 Arthrocare Urologic Multi-Electrode Electrosurgery SystemArthrocare Corp. · 1996
- 7 generations backK962445 Arthrocare Dental Electrosurgery SystemArthrocare Corp. · 1996
- 6 generations backK964849 Arthrocare Dermatologic Electrosurgery SystemArthrocare Corp. · 1997
- 5 generations backK971532 Arthrocare Electrosurgery SystemArthrocare Corp. · 1997
- 4 generations backK974521 Vnus Closure SystemVnus Medical Technologies, Inc. · 1998
- 3 generations backK982816 Vnus Closure SystemVnus Medical Technologies, Inc. · 1999
- 2 generations backK030557 Modification to Vnus Closure SystemVnus Medical Technologies, Inc. · 2003
- 1 generation backK061373 Vnus Closurefast Catheter, Models CF7-7-60 and CF7-7-100Vnus Medical Technologies, Inc. · 2006 · Recalled
- This deviceK111887 Closurefast Radiofrequency CatheterCovidien · 2011
Showing 5 of 6 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 6 · See all- K253918Veineo System (00MEDRF4000TCUS 05CR45iT 06Pedal1St)F Care Systems USA, LLC · 2026 · cites it directly0descendants
- K250688Cedar™ Endovenous Radiofrequency Catheter (ERA-C70-US); Cedar™ Endovenous Radiofrequency…Acotec Scientific Co., Ltd. · 2025 · cites it directly0descendants
- K222997VVR Generator systemStarmed Co., Ltd. · 2023 · cites it directly0descendants
- K223488ClosureFast™ Endovenous Radiofrequency Ablation CatheterMedtronic, Inc. · 2023 · cites it directly0descendants
- K191073Vein360 Endovenous Radiofrequency Ablation (RFA) CatheterVein 360, LLC · 2019 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −9 | K943450 | Arthrocare Arthroscopic Electrosurgery System Model 970 | Arthrocare Corp. | 1995 | — |
| −8 | K961069 | Arthrocare Urologic Multi-Electrode Electrosurgery System | Arthrocare Corp. | 1996 | — |
| −7 | K962445 | Arthrocare Dental Electrosurgery System | Arthrocare Corp. | 1996 | — |
| −6 | K964849 | Arthrocare Dermatologic Electrosurgery System | Arthrocare Corp. | 1997 | — |
| −5 | K971532 | Arthrocare Electrosurgery System | Arthrocare Corp. | 1997 | — |
| −4 | K974521 | Vnus Closure System | Vnus Medical Technologies, Inc. | 1998 | — |
| −3 | K982816 | Vnus Closure System | Vnus Medical Technologies, Inc. | 1999 | — |
| −2 | K030557 | Modification to Vnus Closure System | Vnus Medical Technologies, Inc. | 2003 | — |
| −1 | K061373 | Vnus Closurefast Catheter, Models CF7-7-60 and CF7-7-100 | Vnus Medical Technologies, Inc. | 2006 | 2 |
| 0 (this device) | K111887 | Closurefast Radiofrequency Catheter | Covidien | 2011 | — |
| +1 | K253918 | Veineo System (00MEDRF4000TCUS 05CR45iT 06Pedal1St) | F Care Systems USA, LLC | 2026 | — |
| +1 | K250688 | Cedar™ Endovenous Radiofrequency Catheter (ERA-C70-US); Cedar™ Endovenous… | Acotec Scientific Co., Ltd. | 2025 | — |
| +1 | K222997 | VVR Generator system | Starmed Co., Ltd. | 2023 | — |
| +1 | K223488 | ClosureFast™ Endovenous Radiofrequency Ablation Catheter | Medtronic, Inc. | 2023 | — |
| +1 | K191073 | Vein360 Endovenous Radiofrequency Ablation (RFA) Catheter | Vein 360, LLC | 2019 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1980 | 1 | 0 |
| 1985 | 1 | 0 |
| 1995 | 2 | 0 |
| 1996 | 4 | 0 |
| 1997 | 6 | 0 |
| 2000 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2017 | 1 | 0 |
| 2019 | 1 | 0 |
| 2023 | 2 | 0 |
| 2025 | 1 | 0 |
| 2026 | 1 | 0 |
Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in GEI? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
Top candidate predicates for a new GEI device
- #1 K231790 The InMode System with the Morpheus8 Applicatorsscore 32.7 · 21 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (1)
Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K061373 | Vnus Closurefast Catheter, Models CF7-7-60 and CF7-7-100Summary page 1…Electrosurgical Device F. Classification Name Electrosurgical cutting and coagulation device and accessories G. Predicate Device(s) ClosureFASTrm Catheter (K061373) H. Device Description The ClosureFASflM Radiofrequency Catheter is provided sterile, and is a single-use, disposable d… | 2006 |
What descends from it? (6)
6 later devices cite it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K253918 | Veineo System (00MEDRF4000TCUS 05CR45iT 06Pedal1St) | 2026 | 0 |
| K250688 | Cedar™ Endovenous Radiofrequency Catheter (ERA-C70-US); Cedar™ Endovenous Radiofrequency… | 2025 | 0 |
| K222997 | VVR Generator system | 2023 | 0 |
| K223488 | ClosureFast™ Endovenous Radiofrequency Ablation Catheter | 2023 | 0 |
| K191073 | Vein360 Endovenous Radiofrequency Ablation (RFA) Catheter | 2019 | 0 |
| K172535 | Bipolar applicator CELON ProCurve V | 2017 | 0 |
Has anything in its family been recalled? (0 Class I)
No FDA recall names this device.
No ancestor or descendant has a Class I recall.
What does this lineage say?
- The line of descent spans 16 years and passes through 3 companies; a new generation was cleared every 1.1 years on median.
- 2 of the 24 ancestors have a recall of any class.
- Of its descendants, K253918 (F Care Systems USA, LLC, 2026) has gone furthest, with 0 descendants of its own.
- 5 other devices also cite its predicate K061373.
How does its category compare?
All GEI devicesGEI Electrosurgical, Cutting & Coagulation & Accessories: FDA decisions, review times, recalls and adverse event reports over 20 years. 2011, this device’s year, is highlighted.
FDA decisions per year · GEI
52in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · GEI
113in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · GEI
4in 2025
Class I (14 since 2007) Class II/III not classified
Adverse event reports per year · GEI
7,592in 2025
MAUDE reports naming product code GEI, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 50 | 51 | 21 | 2,795 |
| 2008 | 61 | 71 | 19 | 2,556 |
| 2009 | 42 | 130 | 27 | 3,591 |
| 2010 | 46 | 109 | 51 | 3,377 |
| 2011 | 35 | 135 | 32 | 4,463 |
| 2012 | 39 | 133 | 30 | 5,216 |
| 2013 | 48 | 136 | 13 | 4,897 |
| 2014 | 49 | 103 | 3 | 4,908 |
| 2015 | 47 | 123 | 4 | 4,936 |
| 2016 | 64 | 108 | 3 | 5,616 |
| 2017 | 52 | 72 | 2 | 6,073 |
| 2018 | 47 | 93 | 6 | 6,545 |
| 2019 | 48 | 93 | 5 | 7,067 |
| 2020 | 59 | 105 | 1 | 6,490 |
| 2021 | 46 | 146 | 6 | 6,354 |
| 2022 | 55 | 150 | 49 | 6,103 |
| 2023 | 65 | 104 | 27 (4) | 7,176 |
| 2024 | 59 | 125 | 22 (10) | 7,897 |
| 2025 | 52 | 113 | 4 | 7,592 |
| 2026 | 43 | 183 | 8 | — |
What is it indicated for?
The ClosureFAST m Radiofrequency Catheter is intended for endovascular coagulation of blood vessels in patients with superficial vein reflux.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K111887 · printed Nov 6, 2026
Cite this page
510(k) Report. “K111887: Closurefast Radiofrequency Catheter.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K111887
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Record history
- FDA decision record loaded May 2, 2026
- Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026