Siemens Virtual Simulation (Vsim)
by Siemens Medical Solutions USA, Inc.
510(k) K022036
Siemens Virtual Simulation (Vsim) is a Class II device made by Siemens Medical Solutions USA, Inc., cleared under FDA 510(k) K022036 on 5 Nov 2002, 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 | NumberK022036 | Date5 Nov 2002 | StatusActive |
Official records
- FDA 510(k) database K022036
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- MUJ
- Device class
- Class II
- Regulation
- 21 CFR Part 892.5050
- Advisory committee
- Radiology
- FDA decision
- SESE Substantially Equivalent
Similar devices
Other devices filed under FDA product code MUJ (System, Planning, Radiation Therapy Treatment).
- XPLAN 2.2 WITH THE BODY SYSTEM by Radionics, A Division of Tyco Healthcare Group LP
- ERGO SRS by 3D Line USA, Inc.
- IMAGEFUSION 2.0 by Radionics, Inc.
- CYBERKNIFE ROBOTIC RADIOSURGERY SYSTEM by Accuray, Inc.
- ECLIPSE, HELIOS OPTION by Varian Medical Systems, Inc.
- TrueFit Bolus by ADAPTIIV MEDICAL TECHNOLOGIES, INC.
- RayStation 8.1.2 by RaySearch Laboratories AB (PUBL)
- PlanOne 1 by Cosylab Jsc, Control System Laboratory
- PREFERNCE IMRT TREATMENT PLANNING MODULE by Northwest Medical Physics Equipment, Inc.
- VITESSE 2.0 by Varian Medical Systems, Inc.