The following data is part of a premarket notification filed by Siemens Medical Solutions Usa, Inc. with the FDA for Syngo.ct Myocardial Perfusion.
| Device ID | K150713 |
| 510k Number | K150713 |
| Device Name: | Syngo.CT Myocardial Perfusion |
| Classification | System, X-ray, Tomography, Computed |
| Applicant | SIEMENS MEDICAL SOLUTIONS USA, INC. 51 VALLEY STREAM PARKWAY, MC D02 Malvern, PA 19355 |
| Contact | Eve Davis |
| Correspondent | Kimberly Mangum SIEMENS MEDICAL SOLUTIONS USA, INC. HC CX NAM US QM RA&CA 1 40 Liberty Boulevard Malvern, PA 19355 |
| Product Code | JAK |
| CFR Regulation Number | 892.1750 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2015-03-19 |
| Decision Date | 2015-11-02 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 04056869026435 | K150713 | 000 |
| 04056869013961 | K150713 | 000 |