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U.S. Department of Health and Human Services

510(k) Premarket Notification
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61 to 70 of 185 Results
ProductCode: FPA Applicant: Y Decision Date To: 08/29/2016
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510(K)
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modification to: liftloc saftey infusion set SPECIALTY HEALTH PRODUCTS, INC. K042234 09/08/2004
lily volume meteric administration set, models ib-2111 and cib-120es LILY MEDICAL SUPPLIES CO., LTD. K032767 06/03/2004
ivy devices inc. iv/medical line stabilizer IVY DEVICES, INC. K033208 03/18/2004
ultraflex infusion set DISETRONIC MEDICAL SYSTEMS AG K033892 03/09/2004
signature edition infusion pump, signature edition administration sets, models 70xx, 71xx, 72xx, 7xxxx series ALARIS MEDICAL SYSTEMS, INC. K032147 07/25/2003
bd vacutainer push button blood collection set, models 367338, 367344, 367336, 367342, 367335, 367341 BD VACUTAINER SYSTEMS PREANALYICAL SOLUTIONS K030573 05/08/2003
burette-in line (150 ml) TUTA HEALTHCARE PTY LIMITED K023595 12/18/2002
alaris medical infusion system administration sets ALARIS MEDICAL SYSTEMS, INC. K022209 08/06/2002
modification to 30 extension set CHURCHILL MEDICAL SYSTEMS, INC. K021395 05/13/2002
bd saf-t prn luer activated valve, model 385100 BECTON DICKINSON INFUSION THERAPY SYSTEMS, INC. K013621 04/16/2002
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