Medical Device Recalls
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1 result found
510(K) Number: K203346 |
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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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OEC 3D Imaging, Image-Intensified Fluoroscopic X-Ray System, Mobile - Product Usage: designed to pro... | 2 | 07/29/2021 | GE OEC Medical Systems, Inc |
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