The following data is part of a premarket notification filed by Siemens Ag with the FDA for Syngo.via.
| Device ID | K123375 |
| 510k Number | K123375 |
| Device Name: | SYNGO.VIA |
| Classification | System, Image Processing, Radiological |
| Applicant | SIEMENS AG HENKESTRASSE 127 Erlangen, Bavaria, DE 91052 |
| Contact | Sabine Schroedel |
| Product Code | LLZ |
| CFR Regulation Number | 892.2050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | Yes |
| Combination Product | No |
| Date Received | 2012-11-01 |
| Decision Date | 2012-11-20 |
| Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() SYNGO.VIA 79073846 3811150 Live/Registered |
Siemens Healthcare GmbH 2009-09-01 |