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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K992571
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Celite ACT Cartridge Cartridge is useful for monitoring patients receiving heparin for treatment ... 2 02/16/2011 FEI # 2245578
Abbott Point Of Care Inc.
i-STAT ACT Celite Cartridges in vitro diagnostic test used to monitor moderate and high-level hepar... 2 11/17/2010 FEI # 2245578
Abbott Point Of Care Inc.
Abbott i-STAT ACT Celite Cartridges. In vitro diagnostic test used to monitor moderate and high-l... 2 02/23/2010 FEI # 2245578
Abbott Point of Care Inc.
i-STAT Celite ACT Cartridge. ACT, activated clotting time, celite activated clotting time test. 2 06/21/2005 FEI # 2245578
Abbott Laboratories
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