Medical Device Recalls
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1 result found
510(K) Number: K240465 |
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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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| O-arm O2 Imaging System. Mobile X-Ray System. | 2 | 07/09/2025 |
FEI # 3004785967 Medtronic Navigation, Inc.-Boxborough |
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