Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K162268 |
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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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Senographe Pristina | 2 | 02/08/2024 | GE Medical Systems, SCS |
GE Senographe Pristina - Product Usage: Senographe Pristina generates digital mammographic images th... | 2 | 07/30/2019 | GE Healthcare, LLC |
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