DRP
- Product code
- DRP
- Device name
- Tourniquet, Automatic Rotating
- Device class
- Class 2
- 21 CFR
- 21 CFR 870.5925
- Medical specialty
- Cardiovascular
- Marketing pathway
- 510(K)
- Flag
- Third-party review eligible
Official FDA classification page: DRP
Classification and pathway per current FDA publications. Data from openFDA (CC0).