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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K011093
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FDA Recall
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Intellivue Information Center Model: M3150B#C01 2 02/28/2003 FEI # 1218950
Philips Medical Systems, Inc. Cardiac & Monitoring Systems
Intellivue Information Center Model: M3150BU#CO1 2 02/28/2003 FEI # 1218950
Philips Medical Systems, Inc. Cardiac & Monitoring Systems
Viridia/Agilent Information Center Model : M3150A#C01 2 02/28/2003 FEI # 1218950
Philips Medical Systems, Inc. Cardiac & Monitoring Systems
Viridia/Agilent Information Center Model : M3151A#CO1 2 02/28/2003 FEI # 1218950
Philips Medical Systems, Inc. Cardiac & Monitoring Systems
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