Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K080124 |
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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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System, Tomography Computed Emmission | 2 | 06/03/2020 | GE Healthcare, LLC |
Ventri Discovery NM 530c, Ventri with Premium Table Discovery NM 530c, models H3000ZW & H3000SA. The... | 2 | 04/24/2013 | GE Healthcare, LLC |
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