Medical Device Recalls
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1 result found
510(K) Number: K230179 |
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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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| Esaote Endocavity ultrasonic probe, Model E 3-12, REF 120000038 | 2 | 03/03/2026 |
FEI # 3012981490 ESAOTE S.P.A. |
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