Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K131807 |
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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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Plan Parameters workspace within Eclipse Treatment Planning System Version 11 and 13; ARIA Radiati... | 2 | 12/20/2013 | Varian Medical Systems, Inc. |
C-Series: Clinac, Trilogy, Trilogy Tx. , Novalis high energy linear accelerators and UNIQUE single ... | 2 | 12/03/2013 | Varian Medical Systems, Inc. |
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