Medical Device Recalls
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1 result found
510(K) Number: K851058 |
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Product Description
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Recall
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FDA Recall
Posting Date |
Recalling Firm
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| "***DOSI-FLOW 1 I.V. EXTENSION SET WITH I.V. FLOW REGULATOR REGULADOR DE CAUDAL PARA SETS DE INFUSIO... | 2 | 06/21/2011 | Leventon S. A. U. |
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