Medical Device Recalls
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1 result found
510(K) Number: K771444 |
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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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Qualicheck 1+, Aqueous Quality Control, Level 2, S7140, REF 944-042. The solution is used for qu... | 3 | 12/21/2012 | Radiometer America Inc |
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