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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: K810859
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U-SDN 2 Part Ultra Modified Seldinger Needles, NS/37-0387. All needles were sold in bulk, non-ste... 2 12/01/2015 FEI # 3020778
Procedure Products, Inc.
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