The following data is part of a premarket notification filed by Siemens Medical Solutions Usa, Inc. with the FDA for Syngo.ct Coronary Analysis; Syngo.ct Vascular Analysis.
Device ID | K173637 |
510k Number | K173637 |
Device Name: | Syngo.CT Coronary Analysis; Syngo.CT Vascular Analysis |
Classification | System, X-ray, Tomography, Computed |
Applicant | Siemens Medical Solutions USA, Inc. 40 Liberty Blvd. Malvern, PA 19355 |
Contact | Kimberly Mangum |
Correspondent | Kimberly Mangum Siemens Medical Solutions USA, Inc. 40 Liberty Blvd. 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 | 2017-11-24 |
Decision Date | 2018-03-30 |
Summary: | summary |