Product code
QEW: Peripheral mechanical thrombectomy with aspiration
FDA product code · Class II · Cardiovascular
Key facts
| Product code | QEW |
|---|---|
| Device | Peripheral mechanical thrombectomy with aspiration |
| Device class | Class II |
| Regulation number | 870.5150 |
| Review panel | Cardiovascular |
| Medical specialty | Cardiovascular |
| Submission type | 510(k) |
| GMP exempt | No |
| Implanted device | No |
| Life-sustaining or life-supporting | No |
| Definition | To mechanically disrupt thrombus and/or debris prior to removal from the peripheral vasculature through aspiration. |
At a glance
- 100–999 510(k) clearances
- None De Novo grants
- None PMA approvals
- None HDE approvals
- 100–999 UDI devices (GUDID)
- 1,000+ MAUDE adverse event reports
- 10–99 Recalled products (Z-numbers)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device product codes
FDA product codes classify medical devices by type and intended use; each code maps to a device class, a classification regulation and a review panel.
Source: U.S. Food and Drug Administration (FDA), Product Classification database