Medical Device Recalls
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11 to 12 of 12 Results
510(K) Number: K010817 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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MX8000 Dualv. EXP, 728130. Computed Tomography X-ray systems intended to produce cross-sectional ... | 2 | 05/22/2015 | Philips Medical Systems (Cleveland) Inc |
Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option - Monitor Bracket Assembly for use ... | 2 | 06/30/2021 | Philips North America Llc |
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