| K-number | K922165 |
| Device name | ATC725, ATC525, AND AP300 |
| Applicant | Gendex Corp. |
| Product code | IZO |
| Device class | Class I |
| Decision date | Jul 27, 1992 |
| Decision | Substantially Equivalent |
| Regulation | 892.1700 |
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