Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K040444 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| GE Healthcare MR superconducting magnets, a component of GE SIGNA 3.0T with Excite MR System, nuclea... | 2 | 02/09/2022 |
FEI # 2126677 GE Healthcare, LLC |
| GE Healthcare, SIGNA Excite 3.0T. MR System for use as a diagnostic imaging device. | 2 | 11/10/2015 |
FEI # 2126677 GE Healthcare |
| GE Healthcare-Americas Signa 3.0T EXCITE Whole Body Magnetic Resonance System | 2 | 05/18/2007 |
FEI # 2183553 GE Medical Systems LLC |
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