Medical Device Recalls
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1 result found
510(K) Number: K150235 |
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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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CLEARSIGN II Amplifier for LABSYSTEM PRO EP Recording System, 120 channels, using firmware version ... | 2 | 06/18/2015 | Boston Scientific Corporation |
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