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