The following data is part of a premarket notification filed by Union Carbide Corp. with the FDA for 510 Bedside X-ray System.
| Device ID | K780947 |
| 510k Number | K780947 |
| Device Name: | 510 BEDSIDE X-RAY SYSTEM |
| Classification | System, X-ray, Mobile |
| Applicant | UNION CARBIDE CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | IZL |
| CFR Regulation Number | 892.1720 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1978-06-09 |
| Decision Date | 1978-06-22 |