The following data is part of a premarket notification filed by Siemens Corp. with the FDA for Somatom Sd.
| Device ID | K790342 |
| 510k Number | K790342 |
| Device Name: | SOMATOM SD |
| Classification | System, X-ray, Tomography, Computed |
| Applicant | SIEMENS CORP. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | JAK |
| CFR Regulation Number | 892.1750 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-02-21 |
| Decision Date | 1979-03-22 |