Medical Device Recalls
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1 result found
510(K) Number: K990766 |
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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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| Lumbar Matrix Scan, Diagnostic Electromyography System consisting of the CERSR Electromyography Syst... | 2 | 06/30/2010 |
FEI # 3002881252 SpineMatrix Inc |
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