Lumilisse IPL Hair Remover
K-Number: K172791 · 2018-01-18
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Device Summary
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. The listed applicant is Conair Corporation. The 510(k) number is K172791.
When did Lumilisse IPL Hair Remover receive FDA 510(k) clearance?
Lumilisse IPL Hair Remover received FDA 510(k) clearance on 2018-01-18, under 510(k) number K172791.
Who is the listed applicant for Lumilisse IPL Hair Remover?
The FDA 510(k) record lists Conair Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Lumilisse IPL Hair Remover?
The FDA product code for Lumilisse IPL Hair Remover is OHT.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: OHT)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.
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