Device Type ID | 5376 |
Device Name | Device, Beam Limiting, X-ray, Therapeutic |
Regulation Description | X-ray Radiation Therapy 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 | 892.5900 [🔎] |
FDA Device Classification | Class 2 Medical Device |
Product Code | KQA |
GMP Exempt | No |
Summary MR | Eligible |
Implanted Device | No |
Life Support Device | No |
Third Party Review | Eligible For Accredited Persons Expansion Pilot Program |