Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K091404 |
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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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Reference materials "RETINAL OCT Analysis and Interpretation Method" shipped with iVue System (K0914... | 2 | 10/09/2012 | Optovue Inc. |
Optovue iVue optical coherence tomography system, computer controlled opthalmic imaging system, manu... | 2 | 02/01/2011 | Optovue Inc. |
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