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 |