| K-number | K828543 |
| Device name | UNKNOWN |
| Applicant | General Electric Co. |
| Product code | — |
| Device class | Class unclassified |
| Decision date | Jan 1, 1985 |
| Decision | Substantially Equivalent |
| Regulation | — |
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