The following data is part of a premarket notification filed by Xeroradiography with the FDA for Xeroradiography 125 System - Modified.
| Device ID | K761022 |
| 510k Number | K761022 |
| Device Name: | XERORADIOGRAPHY 125 SYSTEM - MODIFIED |
| Classification | System, Imaging, X-ray, Electrostatic |
| Applicant | XERORADIOGRAPHY 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | IXK |
| CFR Regulation Number | 892.1630 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1976-11-11 |
| Decision Date | 1976-11-24 |