El.En Electronic Engineering Spa
FDA 510(k) medical device clearances.
Top product codes for El.En Electronic Engineering Spa
Recent clearances by El.En Electronic Engineering Spa
- K222221 — DEKA HELIX
- K213658 — DEKA SMARTPERIO
- K212270 — DEKA LipoAI
- K211091 — Deka Tiac II
- K211362 — SCAR 3
- K203396 — DEKA SMARTPERIO
- K211821 — DEKA Motus AZ
- K202258 — ERISE Laser handpiece
- K202079 — Physiq
- K192539 — Deka Luxea
- K181867 — Deka Smartxide2 Trio
- K181510 — ECHOLASER X4
- K181486 — DEKA Motus AY
- K180193 — DEKA SMARTXIDE Family (Smartxide Touch, Smartxide Punto)
- K172362 — DEKA SMARTXIDE TOUCH
- K172363 — DEKA SMARTXIDE ULTRASPEED
- K162886 — DEKA MOTUS AX
- K150516 — DEKA SYNCHRO REPLA:Y FAMILY OF LASER SYSTEMS
- K131095 — DEKA SYNCHRO REPLA: Y FAMILY OF LASER SYSTEMS
- K113504 — DEKA SMARTXIDE AND DELIVERY ACCESSORIES
- K122125 — ASA LASER SH1
- K103288 — DEKA SYNCHRO FT
- K101904 — SMARTXIDE 50 HS/MS
- K082040 — MINISILK FT
- K082039 — SYNCHRO HP PLATFORM
- K072159 — SMART CO2 (SMARTXIDE, SMART US20D) WITH DOT SCANNER
- K062762 — DERMA YAG
Data sourced from openFDA. This site is unofficial and independent of the FDA.