Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K061682 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| GE Voluson¿ E8 Ultrasound System with software versions 6.0.0, 6.0.1,6.1.0, 6.2.0, 6.2.1, 6.2.2, 6.... | 2 | 09/22/2008 | GE Healthcare |
| GE Healthcare Voluson E8 ultrasound scanner with Software version 6.2.0 and 6.2.1 and DICOM stations... | 2 | 11/07/2007 |
FEI # 3005860720 Ge Healthcare |
| GE Healthcare Voluson E6, GE Voluson E8, and GE Voluson E8 Expert Diagnostic Ultrasound Systems | 2 | 12/16/2009 |
FEI # 2126677 GE Medical Systems, LLC |
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