Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K981543 |
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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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| TRACHEAL INTUBATION FIBERSCOPE OLYMPUS LF-GP, Model Number: LF-GP | 2 | 12/14/2023 |
FEI # 2429304 Olympus Corporation of the Americas |
| Rhinolaryngoscope-for endoscopic diagnosis and treatment within the nasal lumens and airway anatomy ... | 2 | 11/17/2023 |
FEI # 3002964398 Aizu Olympus Co., Ltd. |
| Transnasal esophagovideoscope-For endoscopy and endoscopic surgery within the esophagus and stomach.... | 2 | 11/17/2023 |
FEI # 3002964398 Aizu Olympus Co., Ltd. |
| Tracheal fiberscope-airway management, which includes observation to access airway anatomy, endotrac... | 2 | 11/17/2023 |
FEI # 3002964398 Aizu Olympus Co., Ltd. |
| Olympus Tracheal Intubation Fiberscope, Models LF-DP, LF-GP, & LF-TP. | 2 | 08/31/2023 |
FEI # 2429304 Olympus Corporation of the Americas |
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