Medical Device Recalls
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1 result found
510(K) Number: K133882 |
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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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CARESCAPE Central Station - Product Usage: The intended use is to provide clinicians with adult, ped... | 2 | 12/20/2019 | GE Healthcare, LLC |
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