Medical Device Recalls
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1 result found
510(K) Number: K071640 |
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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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VentriClear® II Ventricular Drainage Catheter Set. Allows external access and drainage of cerebrosp... | 2 | 12/14/2015 | Cook Inc. |
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