Medical Device Recalls
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1 result found
510(K) Number: K970586 |
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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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| BrainLab Micro-Multileaf-Collimator, model 41600; BrainLab AG, Kapellenstrasse 12, 85622 Feldkirchen... | 2 | 07/02/2009 | Brainlab AG |
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