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U.S. Department of Health and Human Services

510(k) Premarket Notification
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101 to 110 of 185 Results
ProductCode: FPA Applicant: Y Decision Date To: 04/19/2015
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510(K)
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maxplus tru-swab positive displacement connector MEDEGEN MEDICAL MANUFACTURING SYSTEM K051939 08/01/2005
maxplus tru-swab positive displacement connector MEDEGEN MEDICAL MANUFACTURING SYSTEM K072542 09/25/2007
three way infusion set MED FUSION SYSTEMS, INC. K841882 06/05/1984
mckinley outbound-2 system MCKINLEY, INC. K971844 01/23/1998
i.v. transfer spike LYPHOMED, INC. K842678 10/09/1984
nitroglycerin infusion set LYPHOMED, INC. K853019 11/12/1985
secondary administration set LYPHOMED, INC. K853086 08/19/1985
spark kit(r), modification LYPHOMED, INC. K910142 05/14/1991
vented secondary iv administration set LYPHOMED, INC. K852881 08/16/1985
lily volume meteric administration set, models ib-2111 and cib-120es LILY MEDICAL SUPPLIES CO., LTD. K032767 06/03/2004
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