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Xtreem Pulse

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
3
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K243587PureLift GLOWMarch 6, 2025
K230506PureLift Pro EditionJune 21, 2023
K221443PureLift Pro PlusOctober 21, 2022
K190269PureLiftAugust 28, 2019
K173483Pure Flow External Counter-Pulsation DeviceMay 30, 2018