Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K211312 |
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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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Universal Viewer Workflow Manager, Image processing radiological system | 2 | 10/23/2023 | GE Healthcare |
(1) GE Centricity Universal Viewer 6.0, Model 2088026-9XX; (2) GE Centricity Universal Viewer 7.0, M... | 2 | 08/24/2022 | GE Healthcare, LLC |
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