Medical Device Recalls
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1 result found
510(K) Number: K020728 |
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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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Aesculap(R) - Miethke Shunt System, FT040T - Control Reservoir Set w/Distal Catheter and FT075P 0 Ve... | 2 | 02/12/2013 | Aesculap, Inc. |
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