ClearanceBrief
510(k) K920879 ยท IYE Accelerator, Linear, Medical

BRAINSCAN RADIOSURGERY MODULE

ApplicantBrainlab, West Germany, DE
DecisionSubstantially Equivalent, Dec 29, 1992
ReceivedFeb 26, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K920879

DateFirm and productCodeLinked 510(k)
Sep 20, 2009Brainlab 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
MUJNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.