The following data is part of a premarket notification filed by Siemens Medical Solutions, Inc. with the FDA for Syngo Dual Energy With Extended Functionally.
| Device ID | K073003 |
| 510k Number | K073003 |
| Device Name: | SYNGO DUAL ENERGY WITH EXTENDED FUNCTIONALLY |
| Classification | System, X-ray, Tomography, Computed |
| Applicant | SIEMENS MEDICAL SOLUTIONS, INC. 51 VALLEY STREAM PARKWAY Malvern, PA 19355 |
| Contact | Corrine Mcleod |
| Correspondent | Corrine Mcleod SIEMENS MEDICAL SOLUTIONS, INC. 51 VALLEY STREAM PARKWAY Malvern, PA 19355 |
| Product Code | JAK |
| CFR Regulation Number | 892.1750 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2007-10-24 |
| Decision Date | 2008-02-07 |
| Summary: | summary |