ClearanceBrief
510(k) K071992 ยท IYE Accelerator, Linear, Medical

HIGH-DEFINITION 120 MULTILEAF COLLIMATOR (HD120 MLC)

ApplicantVarian Medical Systems, Palo Alto CA, US
DecisionSubstantially Equivalent, Aug 15, 2007
ReceivedJul 20, 2007
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K071992

DateFirm and productCodeLinked 510(k)
Feb 23, 2012Varian Medical Systems, Inc. Oncology Systems
Varian brand Varian 52-leaf Standard MLC multileaf collimator; Reference/FSCA Identifier: CP-04792; Model Number(s): All models, including H52, H54, H56, HHM; Product is manufactured and distributed
Terminated
IYENone listed
Feb 23, 2012Varian Medical Systems, Inc. Oncology Systems
Varian brand 52-leaf Millennium MLC multileaf collimator; Reference/FSCA Identifier: CP-04792; All models, including H52, H54, H56, HHM; Product is manufactured and distributed by Varian Medical Syste
Terminated
IYENone listed
Aug 22, 2011Varian Medical Systems, Inc. Oncology Systems
High-Definition 120 Multileaf Collimator HD 120 MLC is an accessory x-ray collimator designed to be mounted on Varian Trilogy Tx and Trilogy linear accelerators and is intended to shape s-ray field p
Terminated
IYENone listed
Aug 2, 2008Varian Medical Systems Oncology Systems
High-Definition 120 MultiLeaf Collimator, Medical charged-particle radiation therapy system; Software Version 7.0; Product Code: H56; Accessory to Medical Linear Accelerator.
Terminated
IYENone listed

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