Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K141477 |
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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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Discovery IQ Product Usage: The systems are intended for head and whole body attenuation correct... | 2 | 06/19/2019 | GE Healthcare, LLC |
Discovery IQ 2.0 20cm, 4 ring, Model Number 5432539-22 | 2 | 07/31/2018 | GE Healthcare, LLC |
GE Healthcare Discovery IQ X-ray system | 2 | 06/12/2017 | GE Healthcare, LLC |
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