Medical Device Recalls
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1 result found
510(K) Number: K070970 |
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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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| Penumbra Neuron Delivery Catheter 053, 115 cm/12 cm-- MP, manufactured by Penumbra Inc., Alameda, CA... | 2 | 09/24/2009 |
FEI # 3005168196 Penumbra Inc. |
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