Device Type ID | 5343 |
Device Name | Camera, X-ray, Fluorographic, Cine Or Spot |
Regulation Description | Cine Or Spot Fluorographic X-ray Camera. |
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 | 892.1620 [🔎] |
FDA Device Classification | Class 2 Medical Device |
Product Code | IZJ |
GMP Exempt | No |
Summary MR | Eligible |
Implanted Device | No |
Life Support Device | No |
Third Party Review | Eligible For Accredited Persons Program |