510(k) · Cleared
Recalled · Class III · 2015Smith & Nephew Tumescent Catheter Inversion System, Model 7210023
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Smith & Nephew, Inc. · DWQ Stripper, Vein, External
Cleared on Jul 22, 2004 after a 51-day review. The FDA summary names its predicate without a number. It has been recalled once.
- Decided
- Jul 22, 2004
- Review
- 51 days
- Class
- Class II
- Product code
- DWQ
- Recalls
- 1
- Predicates
- 0
The FDA summary names its predicate without a number.
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 DWQ? 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 DWQ device
- #1 K212894 PhasTIPPscore 3.7 · 3 generations · no Class I recall
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 |
|---|---|---|---|
| * | — | Codman® Disposable Vein Stripper (pre-amendment device) Named without a submission number |
What descends from it?
No later submission names this one as a predicate yet.
Has anything in its family been recalled? (0 Class I)
Recalls of this device
| Date | Class | Recall | Root cause | Reason |
|---|---|---|---|---|
| Feb 24, 2015 | Class III | Z-1294-2015 | Employee error | Mislabeled with an incorrect expiration date |
No ancestor or descendant has a Class I recall.
How does its category compare?
All DWQ devicesDWQ Stripper, Vein, External: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · DWQ
1in 2022
2026 to Oct 25, outlined.
Median 510(k) review, days · DWQ
Too few DWQ 510(k)s in any year since 2007 to give a median.
Recalls per year · DWQ
No recall names DWQ since 2007.
Adverse event reports per year · DWQ
5in 2025
MAUDE reports naming product code DWQ, 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 | 0 | — | 0 | 0 |
| 2008 | 0 | — | 0 | 3 |
| 2009 | 0 | — | 0 | 1 |
| 2010 | 0 | — | 0 | 2 |
| 2011 | 0 | — | 0 | 1 |
| 2012 | 0 | — | 0 | 0 |
| 2013 | 0 | — | 0 | 0 |
| 2014 | 0 | — | 0 | 1 |
| 2015 | 0 | — | 0 | 0 |
| 2016 | 0 | — | 0 | 0 |
| 2017 | 0 | — | 0 | 7 |
| 2018 | 0 | — | 0 | 36 |
| 2019 | 0 | — | 0 | 29 |
| 2020 | 0 | — | 0 | 5 |
| 2021 | 0 | — | 0 | 0 |
| 2022 | 1 | — | 0 | 0 |
| 2023 | 0 | — | 0 | 1 |
| 2024 | 0 | — | 0 | 4 |
| 2025 | 0 | — | 0 | 5 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
The Smith & Nephew Tumescent Catheter Inversion System is intended to provide a system for removal of incompetent greater saphenous veins.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K041453 · printed Nov 6, 2026
Cite this page
510(k) Report. “K041453: Smith & Nephew Tumescent Catheter Inversion System, Model 7210023.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K041453
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Record history
- FDA decision record loaded May 2, 2026
- Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
- Page last updated Nov 3, 2026