QZU
- Product code
- QZU
- Device name
- Temporary Embolization Assist Device, Peripheral
- Device class
- Class 2
- 21 CFR
- 21 CFR 870.3325
- Medical specialty
- Cardiovascular
- Marketing pathway
- 510(K)
- 510(k) clearances (last 3 years)
- 1
- Summaries archived here
- 0 (direct download)
- 510(k) clearances (all years, FDA)
- 1 (all years; only the last 3 years are listed here)
FDA classification definition
A temporary coil embolization assist device is a prescription device intended for temporary use in the vasculature to mechanically assist in the embolization of aneurysms with embolic coils. The device is delivered into the vasculature with an endovascular approach. This device is not intended to be permanently implanted and is removed from the body when the procedure is completed.
510(k) clearances, last 3 years (1)
| Number | Decision date | Applicant | Device name | Summary |
|---|---|---|---|---|
| DEN230064 | 2024-02-21 | Rapid Medical Ltd. | BraidE Embolization Assist Device | — |
Official FDA classification page: QZU
Classification and pathway per current FDA publications. Data from openFDA (CC0).