Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K170823 |
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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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GE Vivid E80 ultrasound system Vivid E80 / E90 / E95 ultrasound system is general-purpose ultraso... | 2 | 09/06/2018 | GE Medical Systems Ultrasound & Primary Care Diagnostics, LL |
GE Vivid E90 ultrasound system Product Usage: Vivid E80 / E90 / E95 ultrasound system is general-... | 2 | 09/06/2018 | GE Medical Systems Ultrasound & Primary Care Diagnostics, LL |
GE Vivid E95 ultrasound system Product The device is intended for use by a qualified physician fo... | 2 | 09/06/2018 | GE Medical Systems Ultrasound & Primary Care Diagnostics, LL |
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