Medical Device Recalls
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1 result found
510(K) Number: K945271 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| ENVOY 500 ISE CALIBRATOR KIT, reference 55117 (contained 6 x 20 mL Calibrator High level and 6 x 20... | 2 | 08/01/2018 |
FEI # 3007662974 ELITech Clinical Systems SAS |
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