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FDA 510(k)

Luma Light System

K-Number: K173436 · 2018-01-30

ApplicantLuma Therapeutics
Decision Date2018-01-30
Product CodeFTC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Luma Light System is a medical device manufactured by Luma Therapeutics. It received FDA 510(k) clearance on 2018-01-30 under approval number K173436. The device is classified under product code FTC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Luma Light System?

Luma Light System is a medical device that received FDA 510(k) clearance on 2018-01-30. It is manufactured by Luma Therapeutics. The 510(k) number is K173436.

When was Luma Light System approved by the FDA?

Luma Light System received FDA 510(k) clearance on 2018-01-30, under approval number K173436.

What company makes Luma Light System?

Luma Light System is manufactured by Luma Therapeutics.

What is the FDA product code for Luma Light System?

The FDA product code for Luma Light System is FTC.

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Official Source

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

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