Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K021163 |
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Product Description
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Recall
Class |
FDA Recall
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Recalling Firm
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25-Hydroxy Vitamin D EIA, Catalog #AC-57F1. Product Usage: The IDS 25-Hydroxy Vitamin D EIA kit ... | 2 | 01/18/2013 | IDS (Immunodiagnostic Systems Ltd.) |
IDS 25-Hydroxy Vitamin D EIA Enzymeimmunoassay for the quantitative determination of 25-hydroxyvitam... | 3 | 10/24/2008 | Immunodiagnostics Systems Inc |
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