Medical Device Recalls
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1 result found
510(K) Number: K123319 |
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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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| Hemostasis Probe, Model: CD-B622LA | 2 | 04/05/2024 |
FEI # 2429304 Olympus Corporation of the Americas |
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