Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K113475 |
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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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COBRA FUSION 150 Ablation System, Catalog # (REF) 700-001 | 2 | 02/14/2019 | AtriCure, Inc. |
COBRA FUSION 50, Ablation System, Catalog # (REF) 700-002 | 2 | 02/14/2019 | AtriCure, Inc. |
COBRA FUSION 150 Ablation System (International Only), Catalog # (REF) 700-001MI | 2 | 02/14/2019 | AtriCure, Inc. |
COBRA FUSION 150 Ablation System, Catalog # (REF) 700-001S | 2 | 02/14/2019 | AtriCure, Inc. |
COBRA Fusion 50 Ablation System, COBRA Fusion 150 Ablation System, and COBRA Fusion Magnetic Retriev... | 2 | 11/22/2016 | AtriCure, Inc. |
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