Medical Device Recalls
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1 result found
510(K) Number: K934592 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Piccolo Xpress chemistry analyzer, Model No. 1100-1001, Software version 2.1.55 (NGA)/3.1.35(Jen II) | 2 | 06/12/2020 |
FEI # 2939693 Abaxis Inc |
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