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Parker Quality & Compliance

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510(k) clearance

SmartIPL_NI System

FDA 510(k) source

510(k) number
K241973
Applicant
Lumenis Be, Ltd.
Decision date
Sep 19, 2026
Date received
Jul 5, 2024
Decision
Substantially Equivalent
Clearance type
Traditional
Product code
GEX
Device type
Powered Laser Surgical Instrument
Device class
Class II
Regulation
21 CFR 878.4810
Advisory committee
General, Plastic Surgery
Statement or summary
Summary
Third party
N
Location
Yokneam Ilit, IL