The following data is part of a premarket notification filed by Siemens Medical Solutions Usa, Inc. with the FDA for Syngo.mr Applications.
Device ID | K182904 |
510k Number | K182904 |
Device Name: | Syngo.MR Applications |
Classification | System, Image Processing, Radiological |
Applicant | Siemens Medical Solutions USA, Inc. 40 Liberty Blvd Mailcode 65-1A Malvern, PA 19355 |
Contact | Cordell L. Fields |
Correspondent | Cordell L. Fields Siemens Medical Solutions USA, Inc. 40 Liberty Blvd Mailcode 65-1A Malvern, PA 19355 |
Product Code | LLZ |
CFR Regulation Number | 892.2050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-10-16 |
Decision Date | 2019-07-05 |