GE Vingmed Ultrasound As
6 FDA 510(k) clearances · Recalling firm
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| Record | Firm | Date |
|---|---|---|
| GE Vivid Ultrasound products, Model Numbers: a) Vivid E90, H45581LB; b) Vivid E95, H45581D recall (Z-2316-2024) | GE Vingmed Ultrasound As | 2024-07-05 |
| GE Vivid Ultrasound products, Model Numbers: a) Vivid S70, H45041SW recall (Z-2317-2024) | GE Vingmed Ultrasound As | 2024-07-05 |
| GE Healthcare Vivid S60, ultrasound device recall (Z-2124-2023) | GE Vingmed Ultrasound As | 2023-07-10 |
| GE Healthcare Vivid S70, ultrasound device recall (Z-2125-2023) | GE Vingmed Ultrasound As | 2023-07-10 |
| GE Healthcare Vivid S60N, ultrasound device recall (Z-2126-2023) | GE Vingmed Ultrasound As | 2023-07-10 |
| GE Healthcare Vivid S70N, ultrasound device recall (Z-2127-2023) | GE Vingmed Ultrasound As | 2023-07-10 |
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Every clearance here is in the API, with alerts when new ones post.