| Device Type ID | 755 |
| Device Name | Tourniquet, Automatic Rotating |
| Regulation Description | Automatic Rotating Tourniquet. |
| Regulation Medical Specialty | Cardiovascular |
| Review Panel | Cardiovascular |
| Premarket Review | Office Of Device Evaluation (ODE) Division Of Cardiovascular Devices (DCD) Peripheral Interventional Devices Branch (PIDB) |
| Submission Type | 510(k) |
| CFR Regulation Number | 870.5925 [🔎] |
| FDA Device Classification | Class 2 Medical Device |
| Product Code | DRP |
| GMP Exempt | No |
| Summary MR | Eligible |
| Implanted Device | No |
| Life Support Device | No |
| Third Party Review | Eligible For Accredited Persons Expansion Pilot Program |
| Device Type ID | 755 |
| Device | Tourniquet, Automatic Rotating |
| Product Code | DRP |
| FDA Device Classification | Class 2 Medical Device |
| Regulation Description | Automatic Rotating Tourniquet. |
| CFR Regulation Number | 870.5925 [🔎] |