Medical Device Recalls
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1 result found
510(K) Number: K812648 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| TUM-E-VAC REF 2075, Rx ONLY, NON STERILE --- Ethox International, Buffalo, NY 14204, USA --- Intend... | 3 | 11/22/2011 |
FEI # 1314417 Ethox International, Inc. |
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