| Device Type ID | 748 |
| Device Name | Monitor, Line Isolation |
| Regulation Description | Line Isolation Monitor. |
| Regulation Medical Specialty | Cardiovascular |
| Review Panel | Cardiovascular |
| Premarket Review | Office Of Device Evaluation (ODE) Division Of Cardiovascular Devices (DCD) Cardiac Diagnostics Devices Branch (CDDB) |
| Submission Type | 510(K) Exempt |
| CFR Regulation Number | 870.2620 [🔎] |
| FDA Device Classification | Class 1 Medical Device |
| Product Code | DRI |
| GMP Exempt | No |
| Summary MR | Eligible |
| Implanted Device | No |
| Life Support Device | No |
| Third Party Review | Not Third Party Eligible |
| Device Type ID | 748 |
| Device | Monitor, Line Isolation |
| Product Code | DRI |
| FDA Device Classification | Class 1 Medical Device |
| Regulation Description | Line Isolation Monitor. |
| CFR Regulation Number | 870.2620 [🔎] |
| Device Problems | |
|---|---|
Air Leak | 1 |
| Total Device Problems | 1 |