Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K223144 |
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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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| Galaxy System (GAL-001). Intended to provide bronchoscopic visualization of and access to patient a... | 2 | 12/20/2024 | Noah Medical |
| Galaxy System (GAL-001) | 2 | 12/18/2024 | Noah Medical |
| Galaxy bronchoscope (Product GALB-001) used with Instructions for use, Part: 10000752, part of the N... | 2 | 12/13/2024 | Noah Medical |
| Galaxy System REF GAL-001 (specifically GAL-019, Wired Controller) The Galaxy System and its acce... | 2 | 05/01/2024 | Noah Medical |
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