Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K162838 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| iCT, Model # 728306, computed tomography x-ray system | 2 | 08/06/2019 | Philips Medical Systems (Cleveland) Inc |
| iCT SP Model # 728311, computed tomography x-ray system | 2 | 08/06/2019 | Philips Medical Systems (Cleveland) Inc |
| Brilliance iCT, 728306 Product Usage: Computed Tomography X-ray systems intended to produce cros... | 2 | 04/13/2019 | Philips Medical Systems (Cleveland) Inc |
| Brilliance iCT Intended to produce images of the head and body by computer reconstruction of x-ra... | 2 | 01/19/2018 | Philips Medical Systems (Cleveland) Inc |
| Philips CT systems labeled as the following: 1. Brilliance iCT, Model Number: 728306. | 2 | 09/19/2025 | Philips North America Llc |
| 728306 Brilliance iCT-Computed Tomography X-ray systems 728305 Brilliance iCT Upgrades | 2 | 08/18/2021 | Philips North America Llc |
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