The following data is part of a premarket notification filed by General Electric Co. with the FDA for Sfx-90 Table/spotfilmer W/fluoricon L200.
| Device ID | K801320 |
| 510k Number | K801320 |
| Device Name: | SFX-90 TABLE/SPOTFILMER W/FLUORICON L200 |
| Classification | System, X-ray, Fluoroscopic, Image-intensified |
| Applicant | GENERAL ELECTRIC CO. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | JAA |
| CFR Regulation Number | 892.1650 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-06-03 |
| Decision Date | 1980-07-21 |