Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K010591 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Olympus Ultrasound Endoscope, Model number: GF-UCT160-OL5 - Product Usage: used for diagnostic ultra... | 2 | 11/27/2020 | Olympus Corporation of the Americas |
| Olympus Ultrasound Endoscope, Model number: GF-UC160P-OL5 - Product Usage: used for diagnostic ultra... | 2 | 11/27/2020 | Olympus Corporation of the Americas |
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