Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K120550 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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CartoUnivu Module, Model: Carto 3 Software versions 3.2.2 and 3.2.3; Catalog No. KT-5400-124 WITH... | 2 | 02/20/2014 | Biosense Webster, Inc. |
20-Pole Eco Cable, Catalog #EM-5050-060 Product Usage: The 20-Pole Eco Cable is intended to be u... | 2 | 03/28/2013 | Biosense Webster, Inc. |
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