The following data is part of a premarket notification filed by General Electric Co. with the FDA for Table, X-ray, Rfx Classical.
| Device ID | K760466 |
| 510k Number | K760466 |
| Device Name: | TABLE, X-RAY, RFX CLASSICAL |
| Classification | Table, Radiographic, Tilting |
| Applicant | GENERAL ELECTRIC CO. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | IXR |
| CFR Regulation Number | 892.1980 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1976-08-18 |
| Decision Date | 1976-08-26 |