NQH

Sensor, Pressure, Aneurysm, Implantable

Product code
NQH
Device name
Sensor, Pressure, Aneurysm, Implantable
Device class
Class 2
21 CFR
21 CFR 870.2855
Medical specialty
Cardiovascular
Marketing pathway
510(K)
Flag
Implant
510(k) clearances (all years, FDA)
5 (all years; only the last 3 years are listed here)

FDA classification definition

This device is intended to measure the pressure in the aneurysm sac during and after an endovascular procedure.

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

Official FDA classification page: NQH
Classification and pathway per current FDA publications. Data from openFDA (CC0).