The Luminance RED Acne Device
K-Number: K220729 · 2022-06-09
ApplicantLuminance Medical Ventures, Inc.
Decision Date2022-06-09
Product CodeOLP
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
The Luminance RED Acne Device is a medical device manufactured by Luminance Medical Ventures, Inc.. It received FDA 510(k) clearance on 2022-06-09 under approval number K220729. The device is classified under product code OLP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the The Luminance RED Acne Device?
The Luminance RED Acne Device is a medical device that received FDA 510(k) clearance on 2022-06-09. It is manufactured by Luminance Medical Ventures, Inc.. The 510(k) number is K220729.
When was The Luminance RED Acne Device approved by the FDA?
The Luminance RED Acne Device received FDA 510(k) clearance on 2022-06-09, under approval number K220729.
What company makes The Luminance RED Acne Device?
The Luminance RED Acne Device is manufactured by Luminance Medical Ventures, Inc..
What is the FDA product code for The Luminance RED Acne Device?
The FDA product code for The Luminance RED Acne Device is OLP.
Related Clinical Trials
Other Devices by Luminance Medical Ventures, Inc.
Related Devices (Code: OLP)
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.