Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K862120 |
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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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Table Patient Step on RFX/SFX, Legacy, and Precision 500D systems | 2 | 05/22/2017 | GE Healthcare, LLC |
Legacy | 2 | 12/23/2016 | GE Healthcare, LLC |
Video Monitor Suspensions that may be on the following Fluoroscopic and Radiographic X-Ray systems: ... | 2 | 01/21/2014 | GE Healthcare, LLC |
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