510(k) K080888 ยท MUJ System, Planning, Radiation Therapy Treatment
MODEIFICATION TO IPLAN RT DOSE
| Applicant | Brainlab AG, Feldkirchen, DE |
| Decision | Substantially Equivalent, Jun 11, 2008 |
| Received | Mar 31, 2008 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K080888
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jan 15, 2015 | Brainlab AG iPlan RT Dose is a stereotactic radiation treatment planning system that is intended for use in stereotactic, conformal, computer planned, Linac based radiation treatment of cranial, head and neck, an Terminated |
MUJ | None listed |
| Jan 15, 2015 | Brainlab AG iPlan RT is a radiation treatment planning system that is intended for use in stereotactic, conformal, computer planned, Linac based radiation treatment of cranial, head and neck, and extracranial les Terminated |
MUJ | None listed |
| Sep 20, 2009 | Brainlab AG BrainLab Radiotherapy Treatment Planning Software;
Catalog number 20610 - Radiosurgery 3.0
Catalog number 20620 - Radiosurgery 3.5 and
Catalog number 20630 - Circular ARC SRS/SRT Planning.
The soft Terminated |
MUJ | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.