| Device Type ID | 867 |
| Device Name | Marker, Cardiopulmonary Bypass (vein Marker) |
| Regulation Description | Vascular Graft Prosthesis. |
| Regulation Medical Specialty | Cardiovascular |
| Review Panel | Cardiovascular |
| Premarket Review | Office Of Device Evaluation (ODE) Division Of Cardiovascular Devices (DCD) Circulatory Support Devices Branch (CSDB) |
| Submission Type | 510(k) |
| CFR Regulation Number | 870.3450 [🔎] |
| FDA Device Classification | Class 2 Medical Device |
| Product Code | MAB |
| GMP Exempt | No |
| Summary MR | Eligible |
| Implanted Device | No |
| Life Support Device | No |
| Third Party Review | Not Third Party Eligible |
| Device Type ID | 867 |
| Device | Marker, Cardiopulmonary Bypass (vein Marker) |
| Product Code | MAB |
| FDA Device Classification | Class 2 Medical Device |
| Regulation Description | Vascular Graft Prosthesis. |
| CFR Regulation Number | 870.3450 [🔎] |