General Electric Co. · Class II · Cleared Jan 9, 1981
| K-number | K802953 |
| Device name | DIGITAL FLUOROGRAPHIC X-RAY SYSTEM |
| Applicant | General Electric Co. |
| Product code | JAA |
| Device class | Class II |
| Decision date | Jan 9, 1981 |
| Decision | Substantially Equivalent |
| Regulation | 892.1650 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov