| Device Type ID | 5382 |
| Device Name | Instrument, Quality-assurance, Radiologic |
| Regulation Description | Radiologic Quality Assurance Instrument. |
| 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 | 892.1940 [🔎] |
| FDA Device Classification | Class 1 Medical Device |
| Product Code | LHO |
| GMP Exempt | Yes |
| Summary MR | Eligible |
| Implanted Device | No |
| Life Support Device | No |
| Third Party Review | Not Third Party Eligible |
| Device Type ID | 5382 |
| Device | Instrument, Quality-assurance, Radiologic |
| Product Code | LHO |
| FDA Device Classification | Class 1 Medical Device |
| Regulation Description | Radiologic Quality Assurance Instrument. |
| CFR Regulation Number | 892.1940 [🔎] |
| Device Problems | |
|---|---|
Unintended Collision | 1 |
Manufacturing, Packaging Or Shipping Problem | 1 |
Device Operates Differently Than Expected | 1 |
| Total Device Problems | 3 |