Medical Device Recalls
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1 result found
510(K) Number: K982689 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| The WinStation Retinal Imager, also known as Merge Eye Station. DCF-1024 & DCF-512 Digital Imaging S... | 2 | 02/25/2019 | Merge Healthcare, Inc. |
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