FDA 510(k) Applications for Medical Device Product Code "NVM"
(Catheter, Angioplasty, Peripheral, Transluminal, Dual-Balloon)

FDA 510(k) Number Applicant Device Name Decision Date
K213915 NuMED Inc. BIB Stent Placement Catheter 01/12/2022
K211134 NuMED, Inc BIB Stent Placement Catheter 05/27/2021
K050857 NUMED, INC. BIB PTA BALLOON CATHETER 07/28/2005
K160889 NUMED, INC. BIB Stent Placement Catheter 05/20/2016
K161451 NUMED, INC. BIB Stent Placement Catheter 09/22/2016


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