Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K945913 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| IRISpec" CA/CB two-part urine chemistry control twin set, Iris Diagnostics part number 800-0074. ... | 3 | 08/01/2012 |
FEI # 2023446 Iris Diagnostics |
| IRISpec CA/ IRISpec CB Two-Part Urine Chemistry Control Twin Set, part no. 800-0074. | 3 | 06/11/2005 |
FEI # 2023446 International Remote Imaging Systems Inc |
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