Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K063400 |
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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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Device brochure, labeled in part : BIO -RAD***L70242709 VARIANT TM II TURBO***Hemoglobin A 1C***Cart... | 2 | 04/06/2011 | Bio-Rad Laboratories Inc |
Bio Rad brand VARIANT II TURBO Hemoglobin A1c Program Reorder Pack, Model Number/Catalog No.: 270-24... | 3 | 02/17/2011 | Bio-Rad Laboratories Inc |
Variant II Turbo Hemoglobin A1c Program, model number 270 2417, manufactured by Bio-Rad Laboratories... | 2 | 02/26/2010 | Bio-Rad Laboratories Inc |
Bio-Rad Variant II TURBO Hemoglobin Testing System with CDM v 4.0, model number 270-2600, Manufactur... | 2 | 03/24/2009 | Bio-Rad Laboratories Inc |
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