The following data is part of a premarket notification filed by Siemens Corp. with the FDA for Vertix 3d-u.
| Device ID | K802200 |
| 510k Number | K802200 |
| Device Name: | VERTIX 3D-U |
| Classification | System, X-ray, Stationary |
| Applicant | SIEMENS CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KPR |
| CFR Regulation Number | 892.1680 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-09-11 |
| Decision Date | 1980-10-23 |