Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K173830 |
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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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MAC VU360, Model Number 2030360-001, Electrocardiograph | 2 | 07/23/2019 | GE Healthcare, LLC |
MAC VU360, Electrocardiograph | 2 | 12/07/2020 | GE Healthcare, LLC |
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