Medical Device Recalls
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1 result found
510(K) Number: K232500 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Lumify Diagnostic Ultrasound System models : 795005, 795161, 989605449841, | 2 | 12/04/2025 | Philips Ultrasound, LLC |
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