Medical Device Recalls
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1 result found
510(K) Number: K904883 |
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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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| Integra NeuroSciences Ventrix Ventricular Tunneling Pressure Monitoring Kit NL950-V and Integra Neur... | 2 | 09/08/2009 |
FEI # 2023988 Integra Neuro Sciences |
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