Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K053253 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Analyzing system consists of a small and portable analyzer and plastic microcuvettes. The microcuvet... | 3 | 12/28/2012 |
FEI # 3003044483 HemoCue AB |
| HemoCue® Urine Albumin Microcuvettes, 25 Microcuvettes HemoCue AB Angelholm, Sweden The quantitat... | 2 | 10/25/2013 |
FEI # 3003044483 HemoCue AB |
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