Medical Device Recalls
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1 result found
510(K) Number: K011812 |
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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 Ventricular Drainage Catheter Set, Cat. No. N-VVDC-01-ABRM Product Usage: The Ventri... | 2 | 08/12/2018 | Cook Inc. |
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