| Device Type ID | 5397 |
| Device Name | Cabinet, X-ray System |
| Regulation Description | Stationary X-ray System. |
| Regulation Medical Specialty | Radiology |
| Review Panel | Radiology |
| Premarket Review | Office Of In Vitro Diagnostics And Radiological Health (OIR) |
| Submission Type | 510(k) |
| CFR Regulation Number | 892.1680 [🔎] |
| FDA Device Classification | Class 2 Medical Device |
| Product Code | MWP |
| 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 | 5397 |
| Device | Cabinet, X-ray System |
| Product Code | MWP |
| FDA Device Classification | Class 2 Medical Device |
| Regulation Description | Stationary X-ray System. |
| CFR Regulation Number | 892.1680 [🔎] |
| Premarket Reviews | ||
|---|---|---|
| Manufacturer | Decision | |
FAXITRON BIOPTICS LLC | ||
SUBSTANTIALLY EQUIVALENT | 4 | |
HOLOGIC, INC. | ||
SUBSTANTIALLY EQUIVALENT | 1 | |