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Rex Medical, L.P.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
8
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K212351Revolution Peripheral Atherectomy SystemDecember 15, 2021
K191419Revolution Peripheral Atherectomy System, Revolution Peripheral Atherectomy GuidewireSeptember 12, 2019
K173389Rex Medical Aspiration PumpJanuary 30, 2018
K143405Option (TM) ELITE Vena Cava Filter 100cm SystemApril 16, 2015
K141617CLEANER ROTATIONAL THROMBECTOMY SYSTEMNovember 14, 2014
K133243OPTION ELITE VENA CAVA FILTER SYSTEMDecember 17, 2013
K060904CLEANER ROTATIONAL THROMBECTOMY SYSTEMApril 28, 2006
K042399MODIFICATION TO SHORT INTRODUCER SHEATHDecember 17, 2004