The following data is part of a premarket notification filed by Siemens Medical Solutions Usa, Inc. with the FDA for Syngo.via Mi Workflows.
| Device ID | K123577 |
| 510k Number | K123577 |
| Device Name: | SYNGO.VIA MI WORKFLOWS |
| Classification | System, Image Processing, Radiological |
| Applicant | SIEMENS MEDICAL SOLUTIONS USA, INC. 810 INNOVATION DR. Knoxville, TN 37932 |
| Contact | Alaine Medio, Rac |
| Correspondent | Alaine Medio, Rac SIEMENS MEDICAL SOLUTIONS USA, INC. 810 INNOVATION DR. Knoxville, TN 37932 |
| Product Code | LLZ |
| CFR Regulation Number | 892.2050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2012-11-20 |
| Decision Date | 2013-01-22 |
| Summary: | summary |