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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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