Esie Apps Suite
by Siemens Medical Solutions USA, Inc. 3 variants
510(k) K141554
Esie Apps Suite is a Class II device made by Siemens Medical Solutions USA, Inc., cleared under FDA 510(k) K141554 on 11 Jul 2014, active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK141554 | Date11 Jul 2014 | StatusActive |
Official records
- FDA 510(k) database K141554
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- LLZ
- Device class
- Class II
- Regulation
- 21 CFR Part 892.2050
- Advisory committee
- Radiology
- FDA decision
- SESE Substantially Equivalent
Similar devices
Other devices filed under FDA product code LLZ (System, Image Processing, Radiological).
- 3Dicom MD by Singular Health Pty, Ltd.
- SYNGO IMAGING (VERSION V31) by Siemens Medi Cal Solutions, Inc.
- VITAL CONNECT 4.1 by Vital Images, Inc.
- 3D Anatomic Models by Ricoh USA, Inc.
- 4D View by GE Medical Systems Ultrasound and Primary Care Diagnostics LLC
- DenSeeMammo by Statlife
- ONDEMAND3D by Cybermed Inc.
- PerfusionGo Plus by Yukun (Beijing) Technology Co., Ltd.
- ORTHO-CMS by Medis Medical Imaging Systems bv
- MFCD 118I by Barco N.V.