The following data is part of a premarket notification filed by Siemens Ag, Medical Solutions with the FDA for Syngo Imaging (version V31).
| Device ID | K081734 |
| 510k Number | K081734 |
| Device Name: | SYNGO IMAGING (VERSION V31) |
| Classification | System, Image Processing, Radiological |
| Applicant | SIEMENS AG, MEDICAL SOLUTIONS HENKESTRASSE 127 Erlangen, DE 91052 |
| Correspondent | Stefan Preiss TUV SUD AMERICA INC. 1775 OLD HIGHWAY 8 NW New Brighton, MN 55112 -1891 |
| Product Code | LLZ |
| CFR Regulation Number | 892.2050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | Yes |
| Combination Product | No |
| Date Received | 2008-06-19 |
| Decision Date | 2008-07-03 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 04056869027739 | K081734 | 000 |
| 04056869027654 | K081734 | 000 |
| 04056869027661 | K081734 | 000 |
| 04056869027678 | K081734 | 000 |
| 04056869027685 | K081734 | 000 |
| 04056869027692 | K081734 | 000 |
| 04056869027708 | K081734 | 000 |
| 04056869027715 | K081734 | 000 |
| 04056869027722 | K081734 | 000 |
| 04056869025926 | K081734 | 000 |