Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Lumilisse IPL Hair Remover

K-Number: K172791 · 2018-01-18

ApplicantConair Corporation
Decision Date2018-01-18
Product CodeOHT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Lumilisse IPL Hair Remover is a medical device manufactured by Conair Corporation. It received FDA 510(k) clearance on 2018-01-18 under approval number K172791. The device is classified under product code OHT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Lumilisse IPL Hair Remover?

Lumilisse IPL Hair Remover is a medical device that received FDA 510(k) clearance on 2018-01-18. It is manufactured by Conair Corporation. The 510(k) number is K172791.

When was Lumilisse IPL Hair Remover approved by the FDA?

Lumilisse IPL Hair Remover received FDA 510(k) clearance on 2018-01-18, under approval number K172791.

What company makes Lumilisse IPL Hair Remover?

Lumilisse IPL Hair Remover is manufactured by Conair Corporation.

What is the FDA product code for Lumilisse IPL Hair Remover?

The FDA product code for Lumilisse IPL Hair Remover is OHT.

Related Devices (Code: OHT)

K162231iPulse SmoothSkin Gold Hair Removal Device, Venus Silk.expertCyden Limited K161089sensiLight MiniEl Global Trade, Ltd. K160968iPulse SmoothSkin Gold Hair Removal DeviceCyden Limited K172181micro IPLEl Global Trade, Ltd. K171433Silk'n InfinityHome Skinovations , Ltd. K170269Hee HR MiniOriental Inspiration Limited

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑