Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K093581 |
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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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GE Healthcare Optima CT580; Discovery RT, CT590 RT X-ray system | 2 | 06/12/2017 | GE Healthcare, LLC |
GE Healthcare Optima CT580/Discovery CT590RT scanners running software version 13BW16.3. The Disc... | 2 | 03/20/2014 | GE Healthcare, LLC |
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