Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K201300 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Mobile airway scope-diagnosis and observation to access airway anatomy, endotracheal/endobronchial i... | 2 | 11/17/2023 | Aizu Olympus Co., Ltd. |
| Olympus Airway Mobilescope, Models MAF-DM2, MAF-GM2, & MAF-TM2. | 2 | 08/31/2023 | Olympus Corporation of the Americas |
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