The following data is part of a premarket notification filed by Siemens Medical Solutions Usa, Inc. with the FDA for Somatom Go.up, Somatom Go.now, Somatom Go.top, Somatom Go.all, Scan&go.
| Device ID | K173632 |
| 510k Number | K173632 |
| Device Name: | SOMATOM Go.Up, SOMATOM Go.Now, SOMATOM Go.Top, SOMATOM Go.All, Scan&GO |
| Classification | System, X-ray, Tomography, Computed |
| Applicant | Siemens Medical Solutions USA, Inc. 40 Liberty Blvd. Malvern, PA 19355 |
| Contact | Kimberly Mangum |
| Correspondent | Kimberly Mangum Siemens Medical Solutions USA, Inc. 40 Liberty Blvd. Malvern, PA 19355 |
| Product Code | JAK |
| CFR Regulation Number | 892.1750 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-11-24 |
| Decision Date | 2018-04-13 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 04056869151595 | K173632 | 000 |
| 04056869151588 | K173632 | 000 |
| 04056869151571 | K173632 | 000 |
| 04056869151564 | K173632 | 000 |