Medical Device Recalls
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1 result found
510(K) Number: K091404 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Optovue iVue optical coherence tomography system, computer controlled opthalmic imaging system, manu... | 2 | 02/01/2011 |
FEI # 3005950902 Optovue Inc. |
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