Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K030513 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| CELL-DYN 1800, list numbers 07H77-01, 07H77-03, manufactured by Abbott Hematology, Santa Clara, CA | 2 | 05/20/2010 |
FEI # 2919069 Abbott Laboratories |
| Abbott - CELL-DYN 1800 System with CELL-DYN 22 Calibrators and the CELL-DYN Calibrators and CELL-DYN... | 2 | 03/13/2008 |
FEI # 2919069 Abbott Laboratories |
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