Medical Device Recalls
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1 result found
510(K) Number: K042880 |
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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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Emission Computed Tomography System Image Process System - Product Usage: intended for general Nucle... | 2 | 01/13/2021 | Philips North America, LLC |
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