The following data is part of a premarket notification filed by Xerox Medical Systems with the FDA for Dental Xeroradiography.
| Device ID | K791014 |
| 510k Number | K791014 |
| Device Name: | DENTAL XERORADIOGRAPHY |
| Classification | Unit, X-ray, Intraoral |
| Applicant | XEROX MEDICAL SYSTEMS 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | EAP |
| CFR Regulation Number | 872.1810 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-06-01 |
| Decision Date | 1979-09-04 |