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FDA 510(k)

reVive Light Therapy LED Cleansing System

K-Number: K221430 · 2022-07-27

Decision Date2022-07-27
Product CodeOHS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

reVive Light Therapy LED Cleansing System is a medical device manufactured by Led Technologies, Inc.. It received FDA 510(k) clearance on 2022-07-27 under approval number K221430. The device is classified under product code OHS. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the reVive Light Therapy LED Cleansing System?

reVive Light Therapy LED Cleansing System is a medical device that received FDA 510(k) clearance on 2022-07-27. It is manufactured by Led Technologies, Inc.. The 510(k) number is K221430.

When was reVive Light Therapy LED Cleansing System approved by the FDA?

reVive Light Therapy LED Cleansing System received FDA 510(k) clearance on 2022-07-27, under approval number K221430.

What company makes reVive Light Therapy LED Cleansing System?

reVive Light Therapy LED Cleansing System is manufactured by Led Technologies, Inc..

What is the FDA product code for reVive Light Therapy LED Cleansing System?

The FDA product code for reVive Light Therapy LED Cleansing System is OHS.

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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.