Medical Device Recalls
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1 result found
510(K) Number: K061683 |
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Product Description
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Recall
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FDA Recall
Posting Date |
Recalling Firm
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| The Tina-Quant Myoglobin Gen. 2 Tests system is an immuno-turbidimetric assay for the quantitative i... | 2 | 08/30/2019 |
FEI # 1823260 Roche Diagnostics Operations, Inc. |
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