The following data is part of a premarket notification filed by General X-ray, Inc. with the FDA for X-ray System.
| Device ID | K780963 |
| 510k Number | K780963 |
| Device Name: | X-RAY SYSTEM |
| Classification | System, Simulation, Radiation Therapy |
| Applicant | GENERAL X-RAY, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KPQ |
| CFR Regulation Number | 892.5840 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1978-06-12 |
| Decision Date | 1978-06-27 |