DRX
- Product code
- DRX
- Device name
- Electrode, Electrocardiograph
- Device class
- Class 2
- 21 CFR
- 21 CFR 870.2360
- Medical specialty
- Cardiovascular
- Marketing pathway
- 510(K) Exempt
- 510(k) clearances (last 3 years)
- 329
Official FDA classification page: DRX
Classification and pathway per current FDA publications. Data from openFDA (CC0).