| Device Type ID | 5313 |
| Device Name | Table, Radiographic, Stationary Top |
| Regulation Description | Radiologic Table. |
| Regulation Medical Specialty | Radiology |
| Review Panel | Radiology |
| Premarket Review | Office Of In Vitro Diagnostics And Radiological Health (OIR) |
| Submission Type | 510(K) Exempt |
| CFR Regulation Number | 892.1980 [🔎] |
| FDA Device Classification | Class 2 Medical Device |
| Product Code | IXQ |
| GMP Exempt | No |
| Summary MR | Eligible |
| Implanted Device | No |
| Life Support Device | No |
| Third Party Review | Not Third Party Eligible |
|
| Device Type ID | 5313 |
| Device | Table, Radiographic, Stationary Top |
| Product Code | IXQ |
| FDA Device Classification | Class 2 Medical Device |
| Regulation Description | Radiologic Table. |
| CFR Regulation Number | 892.1980 [🔎] |
| Device Problems | |
|---|---|
Device Issue | 1 |
| Total Device Problems | 1 |