Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K072047 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| VERO MHI-TM2000 Linear Accelerator System --- Common Name: Medical Linear Accelerator MHI-TM2000 L... | 2 | 03/31/2016 |
FEI # 3006942329 MITSUBISHI HEAVY INDUSTRIES, LTD., HIROSHIMA MACHINERY WORK |
| MHI-TM2000 Linear Accelerator System (Software Version 3.0.0 and after) Intended for radiation ther... | 2 | 03/24/2016 |
FEI # 3006942329 MITSUBISHI HEAVY INDUSTRIES, LTD., HIROSHIMA MACHINERY WORK |
| MHI-TM2000 Linear Accelerator System (Software Version 3.5.0 and 3.5.1) | 2 | 05/01/2015 |
FEI # 3006942329 MITSUBISHI HEAVY INDUSTRIES, LTD., HIROSHIMA MACHINERY WORK |
| VERO Linear Accelerator System, Model Number MHI-TM2000, MHI Identifier M101-14021, Software Version... | 2 | 12/17/2014 |
FEI # 3006942329 MITSUBISHI HEAVY INDUSTRIES, LTD., HIROSHIMA MACHINERY WORK |
| VERO Linear Accelerator System, Model Number MHI-TM2000; Common Name: Medical Linear Accelerator. ... | 2 | 09/16/2014 |
FEI # 3006942329 MITSUBISHI HEAVY INDUSTRIES, LTD., HIROSHIMA MACHINERY WORK |
| MHI-TM2000 Linear Accelerator System, Software Version 3.0.0 revision 13 or earlier; Proprietary an... | 2 | 08/08/2013 |
FEI # 3006942329 MITSUBISHI HEAVY INDUSTRIES, LTD., HIROSHIMA MACHINERY WORK |
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