FDA 510(k) Applications Submitted by El.En. S.p.A

FDA 510(k) Number Submission Date Device Name Applicant
K133895 12/20/2013 DEKA SMARTXIDE LASER SYSTEM EL.EN. S.P.A
K231971 07/03/2023 DEKA PHYSIQ 360 El.En. S.p.A


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