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U.S. Department of Health and Human Services

510(k) Premarket Notification
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141 to 150 of 493 Results
ProductCode: FOZ Decision Date To: 01/23/2022
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Device Name
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510(K)
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plume safety avf needle JMS NORTH AMERICA CORP. K040247 03/03/2004
emmebi central venous catheter kit with lestep safety introducer EMMEBI SRL K043446 02/04/2005
protectiv jelco safety i.v. catheter, model 3600 series MEDIX, INC. K041345 07/22/2004
fibrex catheter patency device MEDICAL DEVICE TECHNOLOGIES, INC. K040427 05/03/2004
cathy sterile disposable i.v. cannula with catheter MYCO MEDICAL SUPPLIES, INC. K042504 01/19/2006
edwards lifesciences vantex central venous catheters with thermistor EDWARDS LIFESCIENCES, LLC. K033250 12/30/2003
modification to: nipro safe touch safety fistula needle NIPRO MEDICAL CORP. K032777 11/14/2003
nexiva closed iv catheter system BECTON DICKINSON INFUSION THERAPY SYSTEMS, INC. K032843 02/27/2004
modification to v-cath poly picc HDC CORP. K033853 01/14/2004
cook five lumen central venous catheter COOK, INC. K032274 02/26/2004
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