QZU

Temporary Embolization Assist Device, Peripheral

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.

Definition text from the FDA device classification database (U.S. federal government work, public domain).

510(k) clearances, last 3 years (1)

Last three years. Most recent: 2024-02-21.

NumberDecision dateApplicantDevice nameSummary
DEN2300642024-02-21Rapid Medical Ltd.BraidE Embolization Assist Device
Official FDA classification page: QZU
Classification and pathway per current FDA publications. Data from openFDA (CC0).