Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K232997 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| EVIS EXERA III Gastrointestinal Videoscope GIF-1TH190. Model Number: GIF-1TH190 | 2 | 12/05/2024 |
FEI # 2429304 Olympus Corporation of the Americas |
| Brand Name: EVIS EXERA III Gastrointestinal Videoscope GIF-1TH190 Product Name: Olympus GIF-1TH190 ... | 2 | 11/20/2024 |
FEI # 2429304 Olympus Corporation of the Americas |
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