Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K051025 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Fluoroscan Mini C-arm InSight, software versions 1.x, 2.x, 3.x The device is a Mini C-arm Flurosc... | 2 | 05/17/2013 | Hologic, Inc. |
| Fluoroscan Mini C-arm InSight2, software versions 3.x, 4.0, 4.0.1, 4.0.2 The device is a Mini C-a... | 2 | 05/17/2013 | Hologic, Inc. |
| Hologic Fluoroscan Mini C-Arm Model with InSight- FD Software Version 5.0.1and 5.0.2 The device i... | 2 | 09/25/2012 | Hologic, Inc. |
| Hologic Fluoroscan Mini C-Arm Model with InSight2, Software version 4.0 and 4.0.1 The device is ... | 2 | 09/25/2012 | Hologic, Inc. |
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