Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K170909 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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INFX-8000V. For radiographic and fluoroscopic studies and intervention. | 2 | 09/02/2022 | Canon Medical System, USA, INC. |
Canon INTERVENTIONAL ANGIOGRAPHY SYSTEM MODEL INFX-8000V Catheterization Table CAT-880B Canon C... | 2 | 03/17/2021 | Canon Medical System, USA, INC. |
System INFX-8000V | 2 | 03/09/2021 | Canon Medical System, USA, INC. |
Infinix-8000V with Catheterization Table CAT-850B or CAT-860B - Product Usage: This device is a digi... | 2 | 06/09/2020 | Canon Medical System, USA, INC. |
INFX-8000V Fluoroscopic X-Ray Systems; INFINIX CF-I/BP PLUS CARDIAC SYSTEM | 2 | 03/02/2018 | Toshiba American Medical Systems Inc |
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