Medical Device Recalls
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1 result found
510(K) Number: K133399 |
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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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CSI Cardiovascular Systems, Inc., Diamondback 360 Peripheral Orbital Atherectomy System, Model Numbe... | 1 | 08/14/2014 | Cardiovascular Systems, Inc. |
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