Medical Device Recalls
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1 result found
510(K) Number: K150975 |
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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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| IntelliVue Multi Measurement Server, IntelliVue Multi Measurement Server SLCP, IntelliVue Multi Meas... | 2 | 12/27/2017 |
FEI # 1218950 Philips Electronics North America Corporation |
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