Medical Device Recalls
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1 result found
510(K) Number: K200304 |
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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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EPIQ CVxi Diagnostic Ultrasound Systems, Product Code: 795232 | 2 | 10/16/2021 | Philips Ultrasound Inc |
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