Medical Device Recalls
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1 result found
510(K) Number: K101111 |
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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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HALO Ultra Ablation Catheter: Rx only; for use only with the Halo Flex Energy generator and accesso... | 2 | 07/06/2011 | Barrx Medical, Inc. |
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