Medical Device Recalls
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1 result found
510(K) Number: K160182 |
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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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Refurbish RIC5-9-D Probe ROHS compliant Ultrasound Probe RIC5-9-D | 2 | 07/12/2019 | GE Healthcare, LLC |
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