Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K110206 |
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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. |
| Aesculap Miethke Shunt System, miniNAV Valve: The Miethke Shunt System is intended to shunt cerebros... | 3 | 12/16/2014 | Aesculap, Inc. |
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