Medical Device Recalls
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1 result found
510(K) Number: K152330 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Expression MR400 MRI Patient Monitoring System Model Number: 866185 Software version number: 01.0... | 2 | 03/31/2020 |
FEI # 1218950 Philips North America, LLC |
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