ClearanceBrief
510(k) K030609 ยท IXI Block, Beam-Shaping, Radiation Therapy

MODULEAF

ApplicantMrc Systems GmbH, Heidelberg, DE
DecisionSubstantially Equivalent, Mar 17, 2003
ReceivedFeb 26, 2003
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K030609

DateFirm and productCodeLinked 510(k)
Mar 7, 2012Siemens Medical Solutions USA, Inc
Siemens mMLC (ModuLeaf) safety bar and trolley label. Siemens Medical Solutions USA, Inc. Concord, CA. The intended use of the Siemens branded mMLC is an accessory used with the Linear Accelerator s
Terminated
IXINone listed

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