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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
510(K) Number: K041688
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Voluson 730 Expert, Voluson 730 Pro, Voluson 730 ProV with software versions 4.0.0, 4.0.1, 4.0.2, 4.... 3 06/27/2006 General Electric Med. Sys. Ultrasound
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