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Lifelines , Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
2
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K172271Trackit T4 EEG AmplifierMay 4, 2018
K151600R-40 EEG AmplifierOctober 23, 2015
K101691LIFELINES PHOTIC STIMULATORAugust 10, 2010
K010460LIFELINES TRACKITMay 14, 2001