Medical Device Recalls
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1 result found
510(K) Number: K032203 |
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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® Hb 201 Microcuvettes, carton/4 boxes/25 pouches of Microcuvettes, HemoCue AB Angelholm, Swe... | 2 | 10/29/2013 | HemoCue AB |
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