Medical Device Recalls
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1 result found
510(K) Number: K103140 |
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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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| Nicolet EEG Wireless Amplifier 32/64 Channel. Catalog/Part Numbers : 515-015400 for the 32 channel a... | 2 | 03/13/2013 |
FEI # 3010611950 Natus Neurology Incorporated |
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