Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K120425 |
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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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PENTARAY NAV HIGH-DENSITY MAPPING CATHETER ELECTRODE EA 22 Rx only STERILE EO - Product Usage: ... | 2 | 06/16/2020 | BIOSENSE WEBSTER |
PENTARAY NAV High-Density Mapping Catheter. | 2 | 12/07/2017 | Biosense Webster, Inc. |
PENTARAY NAV High-Density Mapping Catheter. | 2 | 12/07/2017 | Biosense Webster, Inc. |
Pentaray NAV High-Density Mapping Catheter, Catalog No. D128201, D128202, D128203, D128204, D128205,... | 2 | 04/29/2016 | Biosense Webster, Inc. |
PENTARAY NAV High-Density Mapping Catheter and PENTARAY NAV ECO Catheter, Catalog No. D128201, D1282... | 2 | 03/11/2014 | Biosense Webster, Inc. |
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