Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K090017 |
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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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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 | Biosense Webster, Inc. |
CARTO 3 Systems, Product Code M-4800-01 The intended use of the CARTO 3 System is catheter-based ... | 2 | 03/20/2012 | Biosense Webster, Inc. |
10 ft. Interface Cable, 10 Pin - Shielded Tip Pins to 12 Pin - Blue, Manufacturing Part Number 01287... | 3 | 03/28/2011 | Biosense Webster, Inc. |
CARTO 3 System Interface Cable, 34-pin to 10-pin, Red, 10' - Part Number: D-1286-18; Catalog Number ... | 2 | 01/07/2011 | Biosense Webster, Inc. |
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