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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K103606
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Software correction applies to customers who use the RT Therapist RTT4.2.108 and RT Therapist Conne... 2 04/26/2013 FEI # 2937457
Siemens Medical Solutions USA, Inc
ARTISTE or ONCOR Digital Linear Accelerators with syngo RT Therapist version 4.2/MOSAIQ OIS Systems ... 2 07/24/2012 FEI # 2937457
Siemens Medical Solutions USA, Inc
Siemens-branded linear accelerator with a 550 TxT Treatment Table with a serial number <_ 1894. Sie... 2 05/03/2012 FEI # 2937457
Siemens Medical Solutions USA, Inc
syngo RT Therapist and syngo RT Therapist Connect/MOSAIQ OIS. This correction applies to customers ... 2 01/11/2012 FEI # 2937457
Siemens Medical Solutions USA, Inc
ARTISTE, Accelerator, Linear, Medical The intended use of the SIEMENS branded ARTISTETM family of l... 2 09/23/2016 FEI # 2240869
Siemens Medical Solutions USA, Inc
ARTISTE, ONCOR Avantgarde, ONCOR Impression Plus, ONCOR Expression, PRIMUS, PRIMUS Plus, Syngo RT Th... 2 09/24/2015 FEI # 2240869
Siemens Medical Solutions USA, Inc
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