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Spirit Hair Removal laser Family

K153718 Class II Traditional
Decision Date
2016-02-12
Sponsor / Applicant
Active Optical Systems , Ltd.

Technical Specification

510(k) Submission ID K153718
Product Code GEX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4810
Decision Date 2016-02-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Spirit Hair Removal laser Family received FDA 510(k) clearance under submission number K153718, sponsored by Active Optical Systems , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2016-02-12.

Classification & Regulation

This clearance is catalogued under FDA product code GEX and 21 CFR 878.4810, within the General, Plastic Surgery review panel as a Class II device.