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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K022272
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Medtronic, DLP, DLP Malleable Single Stage Venous Cannulae. Rx Only, Sterilized Using Ethylene Ox... 2 01/18/2012 FEI # 2182208
Medtronic Inc. Cardiac Rhythm Disease Management
Medtronic Venous Cannulae: a) DLP® 20 Fr. Malleable Single Stage Venous Cannula, Model Number 681... 2 05/10/2024 FEI # 1000116158
Medtronic Perfusion Systems
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