QEY
- Product code
- QEY
- Device name
- Mechanical Thrombolysis Catheter
- Device class
- Class 2
- 21 CFR
- 21 CFR 870.5150
- Medical specialty
- Cardiovascular
- Marketing pathway
- 510(K)
- 510(k) clearances (last 3 years)
- 3
- Summaries archived here
- 3 (direct download)
- 510(k) clearances (all years, FDA)
- 71 (all years; only the last 3 years are listed here)
FDA classification definition
To mechanically disrupt thrombus and/or debris in the peripheral vasculature.
510(k) clearances, last 3 years (3)
| Number | Decision date | Applicant | Device name | Summary |
|---|---|---|---|---|
| K260149 | 2026-02-17 | Liquet Medical, Inc. | Versus Catheter (VS110-9NB) | |
| K251318 | 2026-01-20 | Argon Medical Devices, Inc. | VariFuse Adjustable Infusion Catheter | |
| K241851 | 2024-11-25 | Liquet Medical, Inc. | Versus Catheter (VS110-8B) |
Official FDA classification page: QEY
Classification and pathway per current FDA publications. Data from openFDA (CC0).