Medical Device Recalls
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11 to 12 of 12 Results
510(K) Number: K013636 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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This correction applies to all GE Healthcare MRI systems with superconducting magnets: Discovery MR4... | 1 | 02/18/2015 | GE Healthcare |
Various GE Magnetic Resonance System on-site software version Product Usage: Magnetic resonance ... | 2 | 01/07/2019 | GE Healthcare, LLC |
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