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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K001796
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Recall
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FDA Recall
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Intera MRI 2 06/27/2007 FEI # 1000524572
Philips Medical Systems North America Co. Phillips
NT Intera Magnetic Resonance Image System 2 09/29/2004 FEI # 1000524572
Philips Medical Systems Sales & Service Region No. America
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