Medical Device Recalls
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1 result found
510(K) Number: K954021 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Codman External Drainage System 3 CSF (EDS 3) With Ventricular Catheter Catalog Numer: 82-1730 | 2 | 09/29/2006 |
FEI # 3002947440 Codman & Shurtleff, Inc. |
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