Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K111106 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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TrueBeam and TrueBeam STx V1.0, 1.5, 1.6.95 and below. TrueBeam Radiotherapy Delivery System is inte... | 2 | 05/16/2012 | Varian Medical Systems, Inc. Oncology Systems |
True Beam; Versions 1.0, 1.5.12.0 and below, 1.6.9.5 and below. Varian Medical Systems, Palo Al... | 2 | 05/08/2012 | Varian Medical Systems, Inc. Oncology Systems |
TrueBeam and True Beam STx versions 1.0 through 1.5, Model number H19; Varian Medical Systems, Palo,... | 2 | 03/06/2012 | Varian Medical Systems, Inc. Oncology Systems |
4D Integrated Treatment Console (4DITC) TrueBeam Linear Accelerator Varian Medical Systems, Palo Al... | 2 | 01/11/2012 | Varian Medical Systems, Inc. Oncology Systems |
TrueBeam and TrueBeam STx, Model Number: H19, Ref/FSCA identifier: CP-06381 are intended to provide ... | 2 | 12/02/2011 | Varian Medical Systems, Inc. Oncology Systems |
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