| K-number | K802047 |
| Device name | AMX-III |
| Applicant | General Electric Co. |
| Product code | IZL |
| Device class | Class II |
| Decision date | Oct 23, 1980 |
| Decision | Substantially Equivalent |
| Regulation | 892.1720 |
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