Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K981543 |
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Results per Page |
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 | Olympus Corporation of the Americas |
Olympus Tracheal Intubation Fiberscope, Models LF-DP, LF-GP, & LF-TP. | 2 | 08/31/2023 | Olympus Corporation of the Americas |
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