The following data is part of a premarket notification filed by Siemens Corp. with the FDA for Koordinat 3d.
| Device ID | K790783 |
| 510k Number | K790783 |
| Device Name: | KOORDINAT 3D |
| Classification | Table, Radiologic |
| Applicant | SIEMENS CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KXJ |
| CFR Regulation Number | 892.1980 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-04-23 |
| Decision Date | 1979-05-07 |