The following data is part of a premarket notification filed by Siemens Medical Solutions Usa, Inc. with the FDA for Somatom X.cite, Scan&go, Somatom Go.platform - Go.up, Go.now, Go.top, Go.all, Go. Sim, Go. Open Pro, Scan&go.
| Device ID | K200524 |
| 510k Number | K200524 |
| Device Name: | SOMATOM X.cite, Scan&GO, SOMATOM Go.Platform - Go.Up, Go.Now, Go.Top, Go.All, Go. Sim, Go. Open Pro, Scan&GO |
| Classification | System, X-ray, Tomography, Computed |
| Applicant | Siemens Medical Solutions USA, Inc. 810 Innovation Drive Knoxville, TN 37932 |
| Contact | Tabitha Estes |
| Correspondent | Tabitha Estes Siemens Medical Solutions USA, Inc. 810 Innovation Drive Knoxville, TN 37932 |
| Product Code | JAK |
| CFR Regulation Number | 892.1750 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2020-03-02 |
| Decision Date | 2020-04-01 |