Medical Device Recalls
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1 result found
510(K) Number: K130656 |
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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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iFusion, Device Listing Number D203271. Product Usage: The iCam is a non-contact, high resolutio... | 2 | 10/04/2017 | Optovue, Inc. |
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