FDA 510(k) Applications Submitted by JESSICA OSWALD-MCLEOD

FDA 510(k) Number Submission Date Device Name Applicant
K130049 01/08/2013 MONOJECT 12ML SYRINGE NIPRO MEDICAL CORPORATION
K140136 01/17/2014 NIPRO SAFETOUCH PSV SCALP VEIN SET WITH SAFETY DEVICE NIPRO MEDICAL CORPORATION
K160444 02/17/2016 FB-U Hemodialyzer NIPRO MEDICAL CORPORATION
K151141 04/29/2015 Cronus HP - High Pressure Peripheral Balloon Catheter NIPRO MEDICAL CORPORATION
K191359 05/21/2019 Nipro Syringe Nipro Medical Corporation
K131641 06/04/2013 MONOJECT 60ML SYRINGE (LUER LOCK TIP, LUER SLIP TIP, CATHETER TIP) NIPRO MEDICAL CORPORATION
K161681 06/17/2016 Nipro SafeTouch IV Catheter NIPRO MEDICAL CORPORATION
K132153 07/12/2013 SAFETOUCH PSV WINGED INFUSION SET WITH/WITHOUT FILTER NIPRO MEDICAL CORPORATION
K212677 08/24/2021 aboNT SYRINGE Nipro Medical Corporation
K222852 09/21/2022 Nipro SafeTouch Needle; Nipro Syringe with SafeTouch Needle Nipro Medical Corporation
K173029 09/28/2017 Nipro Syringe Nipro Medical Corporation
K182940 10/23/2018 Surdial DX Hemodialysis System Nipro Medical Corporation


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