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FDA 510(k)

LG PRA.L DERMA LED MASK

K-Number: K183671 · 2019-01-22

ApplicantLg Electronics.Inc
Decision Date2019-01-22
Product CodeOHS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LG PRA.L DERMA LED MASK is a medical device manufactured by Lg Electronics.Inc. It received FDA 510(k) clearance on 2019-01-22 under approval number K183671. 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 LG PRA.L DERMA LED MASK?

LG PRA.L DERMA LED MASK is a medical device that received FDA 510(k) clearance on 2019-01-22. It is manufactured by Lg Electronics.Inc. The 510(k) number is K183671.

When was LG PRA.L DERMA LED MASK approved by the FDA?

LG PRA.L DERMA LED MASK received FDA 510(k) clearance on 2019-01-22, under approval number K183671.

What company makes LG PRA.L DERMA LED MASK?

LG PRA.L DERMA LED MASK is manufactured by Lg Electronics.Inc.

What is the FDA product code for LG PRA.L DERMA LED MASK?

The FDA product code for LG PRA.L DERMA LED MASK is OHS.

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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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