Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K011434 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| G7 HPLC. Used as an aid in the detection and presumptive identification of abnormal hemoglobins i... | 3 | 04/10/2013 | Tosoh Bioscience Inc |
| G7 Variant Elution Buffer HiS no. 1 (M) component of the Tosoh Automated Glycohemoglobin Analyzer HL... | 3 | 07/14/2015 | Tosoh Bioscience, Inc. |
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