Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K133892 |
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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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iVue 500 with iScan, D216606. Product non-contact, high resolution tomographic imaging device. I... | 2 | 10/04/2017 | Optovue, Inc. |
iVue and iVue 500 (now called iScan) OCT systems with software version 2016.0.0.127 (USA only) and 2... | 2 | 08/14/2017 | Optovue, Inc. |
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