DRI
- Product code
- DRI
- Device name
- Monitor, Line Isolation
- Device class
- Class 1
- 21 CFR
- 21 CFR 870.2620
- Medical specialty
- Cardiovascular
- Marketing pathway
- 510(K) Exempt
- 510(k) clearances (all years, FDA)
- 4 (all years; only the last 3 years are listed here)
Official FDA classification page: DRI
Classification and pathway per current FDA publications. Data from openFDA (CC0).