Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K142361 |
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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 MR750 3.0T Product Usage: Intended use: The Discovery MR750 3.0Tsystem is a whole body... | 2 | 08/02/2017 | GE Medical Systems, LLC |
GE Healthcare, Discovery 3.0T MR750, 5148810-2, 5373011-2, 5499460-2. | 2 | 12/28/2015 | GE Medical Systems, LLC |
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