DRO
- Product code
- DRO
- Device name
- Pacemaker, Cardiac, External Transcutaneous (Non-Invasive)
- Device class
- Class 2
- 21 CFR
- 21 CFR 870.5550
- Medical specialty
- Cardiovascular
- Marketing pathway
- 510(K)
- Flag
- Life-sustaining / life-supporting
- 510(k) clearances (all years, FDA)
- 84 (all years; only the last 3 years are listed here)
Official FDA classification page: DRO
Classification and pathway per current FDA publications. Data from openFDA (CC0).