Medical Device Recalls
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1 result found
510(K) Number: K994413 |
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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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BrainLab Radiotherapy Treatment Planning Software; Catalog number 20610 - Radiosurgery 3.0 Cata... | 2 | 09/20/2009 | Brainlab AG |
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