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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
510(K) Number: K043179
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Medtronic Select 3D Arterial Cannulae. Vented, models 78618 (18 Fr.) and 78620 (20 Fr.). Non-Vent... 2 02/20/2014 FEI # 2182208
Medtronic Inc. Cardiac Rhythm Disease Management
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