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U.S. Department of Health and Human Services

510(k) Premarket Notification
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111 to 120 of 185 Results
ProductCode: FPA Applicant: Y Decision Date To: 04/19/2015
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510(K)
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sideport pinch clamp device MEDIVICE SYSTEMS, LTD. K010888 06/27/2001
pressure activated check valve CHURCHILL MEDICAL SYSTEMS, INC. K011888 09/10/2001
vented vial access device CHURCHILL MEDICAL SYSTEMS, INC. K013950 01/10/2002
wing safe infusion set 20 ga, shs2000 series; wing safe infusion set 19 ga, shs1900 series; wing safe infusion set 22 ga CHURCHILL MEDICAL SYSTEMS, INC. K020544 03/12/2002
universal vial access spike with needleless connector CHURCHILL MEDICAL SYSTEMS, INC. K013949 03/27/2002
bd saf-t prn luer activated valve, model 385100 BECTON DICKINSON INFUSION THERAPY SYSTEMS, INC. K013621 04/16/2002
modification to 30 extension set CHURCHILL MEDICAL SYSTEMS, INC. K021395 05/13/2002
alaris medical infusion system administration sets ALARIS MEDICAL SYSTEMS, INC. K022209 08/06/2002
burette-in line (150 ml) TUTA HEALTHCARE PTY LIMITED K023595 12/18/2002
bd vacutainer push button blood collection set, models 367338, 367344, 367336, 367342, 367335, 367341 BD VACUTAINER SYSTEMS PREANALYICAL SOLUTIONS K030573 05/08/2003
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