Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K062927 |
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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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MICroSTREP plus 2 Panel, Part No. B1027-202 Product Usage: MicroScan MICroSTREP plus panels are ... | 2 | 10/07/2015 | Beckman Coulter Inc. |
MICroSTREP plus 1 Panel, Part No. B1027-201 Product Usage: MicroScan MICroSTREP plus panels are ... | 2 | 10/07/2015 | Beckman Coulter Inc. |
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