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Qxmedical, LLC

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
4
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K200317Support CatheterMay 14, 2020
K183679Occlusion Balloon CatheterApril 24, 2019
K160561Boosting CatheterNovember 2, 2016
K123311QXMEDICAL ACCESS & SUPPORT CATHETERJanuary 14, 2013
K120381Q50 PLUS STENT GRAFT BALLOON CATHETERFebruary 24, 2012