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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K103153
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FDA Recall
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NC Trek RX Coronary Dilatation Catheter, Part No. 1012448-06, 1012448-08, 1012448-12, 1012448-15, 10... 1 05/12/2017 FEI # 2024168
Abbott Vascular
NC Tenku RX PTCA Balloon Catheter, Part No. 1012448-08T, 1012448-12T, 1012448-15T, 1012449-08T, 101... 1 05/12/2017 FEI # 2024168
Abbott Vascular
NC Traveler RX Coronary Dilatation Catheter, Part No. 1013152-12, 1013152-15, 1013152-20, 1013153-0... 1 05/12/2017 FEI # 2024168
Abbott Vascular
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