FDA 510(k) Applications Submitted by Lifelines Ltd.

FDA 510(k) Number Submission Date Device Name Applicant
K010460 02/16/2001 LIFELINES TRACKIT LIFELINES LTD.
K101691 06/16/2010 LIFELINES PHOTIC STIMULATOR LIFELINES LTD.
K151600 06/12/2015 R-40 EEG Amplifier LIFELINES LTD.
K172271 07/28/2017 Trackit T4 EEG Amplifier Lifelines Ltd.


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