Medical Device Recalls
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1 result found
510(K) Number: K041074 |
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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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BD Flow Cytometers; used on all BD FACSCount, BD FACSCalibur, BD FACSCanto, BD FACSCanto II, BD LSR ... | 3 | 07/16/2015 | BD Biosciences, Systems & Reagents |
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