The following data is part of a premarket notification filed by Siemens Corp. with the FDA for Sidos U..
| Device ID | K803124 |
| 510k Number | K803124 |
| Device Name: | SIDOS U. |
| Classification | System, Simulation, Radiation Therapy |
| Applicant | SIEMENS CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KPQ |
| CFR Regulation Number | 892.5840 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-12-11 |
| Decision Date | 1981-01-22 |