Medical Device Recalls
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1 result found
510(K) Number: K093304 |
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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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EPWorks software used in the Protektor 32 Product Usage: Uses electroencephalography (EEG), evok... | 2 | 02/09/2015 | Natus Medical Incorporated |
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