Medical Device Recalls
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1 result found
510(K) Number: K103646 |
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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 MX40 Wearable Patient Monitor in use with the Philips IntelliVue Information Center iX (P... | 2 | 06/10/2014 | Philips Medical Systems, Inc. |
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