Medical Device Recalls
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1 result found
510(K) Number: K051417 |
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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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Bard PowerLine 6 Fr. Dual-Lumen Polyurethane Catheter with SureCuff Ingrowth Cuff, REF 0700610, Ster... | 2 | 07/11/2011 | Bard Access Systems |
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