Medical Device Recalls
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1 result found
510(K) Number: K083125 |
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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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Penumbra Neuron 5F Select Catheter, Neuro Deliver/Intracranial Access System Catheter, manufactured ... | 1 | 09/08/2009 | Penumbra Inc. |
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