Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K172550 |
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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 Elite Systems with 9-inch Image Intensifier | 2 | 07/31/2023 | GE OEC Medical Systems, Inc |
OEC Elite mobile C-arm - Product Usage: intended to provide fluoroscopic and digital spot images of ... | 2 | 07/29/2021 | GE OEC Medical Systems, Inc |
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