Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K932166 |
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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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| Duravent Silicone Ventilation Tube. Model Number: 240075. | 2 | 12/19/2024 |
FEI # 2429304 Olympus Corporation of the Americas |
| Olympus/Gyrus Paparrela-Type Vent Tube 1.02MM, Silicone, Sterile- to ventilate the middle ear subseq... | 2 | 02/07/2024 |
FEI # 2429304 Olympus Corporation of the Americas |
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