Medical Device Recalls
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1 result found
510(K) Number: K061129 |
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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 9 ultrasound system Product Usage: The device is intended for use by a qualified phys... | 2 | 09/06/2018 | GE Medical Systems Ultrasound & Primary Care Diagnostics, LL |
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