Nucletron gets 510(k) for Simulix Evolution

AuntMinnie.com staff writers
Feb 9, 2004

Radiotherapy provider Nucletron has received Food and Drug Administration 510(k) marketing clearance for its Simulix Evolution digital simulator.

The product, available as a complete system or as an upgrade for existing Simulix systems, is designed for integrated planning, verification, and simulation of radiation therapy. It is already in clinical use in various clinics in Europe, according to the Veenendaal, Netherlands-based firm.

Simulix Evolution also includes a PC-based simulator workstation, Simplicity, that integrates image handling, plan setup and verification, as well as image and plan import/export. The system features open architecture based on DICOM-RT and RTP-link standards for full connectivity to other radiotherapy systems, including those of many other vendors, Nucletron said.

By AuntMinnie.com staff writers
February 10, 2004

Related Reading

Nucletron, RaySearch partner on IMRT, January 20, 2004

Nucletron gets FDA clearance for Swift, August 21, 2003

Siemens and Nucletron to partner, August 7, 2003

Nucletron books 1,000th Simulix sale, April 10, 2003

Nucletron adds Merry X-Ray, December 10, 2002

Copyright © 2004 AuntMinnie.com

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