The following data is part of a premarket notification filed by Siemens Medical Solutions with the FDA for Inspace 4d Software Package With Extended Functionality.
| Device ID | K071513 |
| 510k Number | K071513 |
| Device Name: | INSPACE 4D SOFTWARE PACKAGE WITH EXTENDED FUNCTIONALITY |
| Classification | System, X-ray, Tomography, Computed |
| Applicant | SIEMENS MEDICAL SOLUTIONS SIEMENSSTRASSE 1 Forchheim, DE D-91301 |
| Contact | Ralf Hofmann |
| Correspondent | Stefan Preiss TUV SUD AMERICA INC. 1775 OLD HIGHWAY 8 NW New Brighton, MN 55112 -1891 |
| Product Code | JAK |
| CFR Regulation Number | 892.1750 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | Yes |
| Combination Product | No |
| Date Received | 2007-06-04 |
| Decision Date | 2007-06-26 |
| Summary: | summary |