510(k) K982713 ยท IYE Accelerator, Linear, Medical
RT DESKTOP
| Applicant | Elekta Oncology Systems, Ltd., Atlanta GA, US |
| Decision | Substantially Equivalent, Nov 2, 1998 |
| Received | Aug 4, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K982713
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Mar 6, 2014 | Elekta, Inc. RT Desktop
The EOS RT Desktop, as with the predicate SL/SLi Series user interface, is intended to be used as the user interface for the SL/SLi Series Linear Accelerators that are used for the radiati Terminated |
IYE | None listed |
| Mar 4, 2011 | Elekta, Inc. Desktop Pro 4.2, 5.0, 5.1, 6.0, 6.2
A user interface of rthe SL/SLi Series Linear Accelerators that are used for radiation therapy treatments of malignant neoplastic diseases, as determined by a lice Terminated |
IYE | None listed |
| Feb 7, 2007 | Elekta, Inc. Desktop Pro R6.0 & R6.1, Linear Medical Accelerator. Terminated |
IYE | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.