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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: K153281
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BrightMatter Guide, Product Number SYN-0026, Versions: 1.5.0, 1.5.1 and 1.5.2 Product Usage: Bri... 1 11/26/2018 FEI # 3012075008
Synaptive Medical Inc
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