Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K110943 |
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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 LOGIQ E9 ultrasound system Product Usage: The device is intended for use by a qualified physi... | 2 | 09/06/2018 | GE Medical Systems Ultrasound & Primary Care Diagnostics, LL |
GE LOGIQ E9 Diagnostic Ultrasound Systems running software versions R3.1.0 and R3.1.1. The device... | 2 | 01/11/2012 | GE Healthcare, LLC |
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