DXY
- Product code
- DXY
- Device name
- Implantable Pacemaker Pulse-Generator
- Device class
- Class 3
- 21 CFR
- 21 CFR 870.3610
- Medical specialty
- Cardiovascular
- Marketing pathway
- PMA
- Flag
- Implant
- 510(k) clearances (all years, FDA)
- 461 (all years; only the last 3 years are listed here)
Official FDA classification page: DXY
Classification and pathway per current FDA publications. Data from openFDA (CC0).