FDA 510(k) Applications Submitted by THERADOME INC.

FDA 510(k) Number Submission Date Device Name Applicant
K122950 09/25/2012 LASER HELMET THERADOME INC.
K113097 10/19/2011 LASER HELMET THERADOME INC.
K171775 06/14/2017 Theradome LH80 PRO Theradome Inc.


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