Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K042861 |
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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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Odyssey A radiation treatment planning system | 2 | 12/01/2011 | PerMedics, Inc. |
Odyssey Intended use: Radiation treatment planning system | 2 | 05/18/2010 | PerMedics, Inc. |
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