Medical Device Recalls
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1 result found
510(K) Number: K031303 |
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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 Inc.(AIC) Miethke Ventricular Catheter with Deflector/Miethke Shunt System The Miethke ... | 2 | 06/02/2014 | Aesculap, Inc. |
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