DRP — Tourniquet, Automatic Rotating Class II
FDA product code DRP covers "Tourniquet, Automatic Rotating", a Class II medical device regulated under 21 CFR 870.5925. Submissions are reviewed by the Cardiovascular panel.
Classification Details
- Product Code
- DRP
- Device Class
- Class II
- Regulation Number
- 870.5925
- Submission Type
- Review Panel
- CV
- Medical Specialty
- Cardiovascular
- Implant
- No