Medical Device Recalls
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1 result found
510(K) Number: K041234 |
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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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HEMOCUE AB Hb 201 DM ANALYZER, in vitro diagnostic device for quantitative hemoglobin determination.... | 2 | 03/30/2011 | Hemo Cue, Inc. |
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