Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K913929 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Merge Eye Station f/k/a: DFC-1024 & DFC-512 Digital Imaging System, WinStation, and WinStation Ret... | 2 | 01/12/2017 |
FEI # 1000116130 Merge Healthcare, Inc. |
| Merge Eye Station. f/k/a: DFC-1024 & DFC-512 Digital Imaging System, WinStation, and WinStation R... | 2 | 02/06/2017 |
FEI # 1000116130 Merge Healthcare, Inc. |
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