Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K152257 |
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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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FUJINON ED-530XT. This device is intended for the visualization of the duodenum and upper digesti... | 2 | 09/27/2017 | Fujifilm Medical Systems U.S.A., Inc. |
Fujifilm Endoscope Model ED-530XT Product Usage: This product is a medical endoscope for the... | 2 | 09/13/2017 | Fujifilm Medical Systems U.S.A., Inc. |
Fujifilm Endoscope Models ED-250XL5 ED-250XT5 ED-450XT5 ED-450XL5 Product Usage: This p... | 2 | 09/13/2017 | Fujifilm Medical Systems U.S.A., Inc. |
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