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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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