Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K013617 |
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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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| Olympus Pleuravideoscope, Model LTF-240 | 2 | 04/22/2020 | Olympus Corporation of the Americas |
| Olympus Pleuravideoscope, Model LTF-160 | 2 | 04/22/2020 | Olympus Corporation of the Americas |
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