The following data is part of a premarket notification filed by General Electric Co. with the FDA for Scx System.
| Device ID | K862120 |
| 510k Number | K862120 |
| Device Name: | SCX SYSTEM |
| Classification | System, X-ray, Fluoroscopic, Image-intensified |
| Applicant | GENERAL ELECTRIC CO. P.O. BOX 414 Milwaukee, WI 53201 |
| Contact | Howard, Ii |
| Correspondent | Howard, Ii GENERAL ELECTRIC CO. P.O. BOX 414 Milwaukee, WI 53201 |
| Product Code | JAA |
| CFR Regulation Number | 892.1650 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1986-06-03 |
| Decision Date | 1986-06-16 |