Medical Device Recalls
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1 result found
510(K) Number: K020860 |
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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 M3 Micro-Multileaf-Collimator for Siemens Mevatron Digital Type III with MLC, model 41600-5... | 2 | 07/02/2009 |
FEI # 3002619595 Brainlab AG |
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