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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
Recall Number: Z-2369-2012
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CARTO 3 V1.05(FG-5400-00). The CARTO 3 V1.05 System is intended for catheter-based atrial and ven... 2 09/12/2012 FEI # 3003113629
Biosense Webster, Inc.
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