LG PRA.L DERMA LED MASK
K-Number: K183671 · 2019-01-22
Device Summary
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. The listed applicant is Lg Electronics.Inc. The 510(k) number is K183671.
When did LG PRA.L DERMA LED MASK receive FDA 510(k) clearance?
LG PRA.L DERMA LED MASK received FDA 510(k) clearance on 2019-01-22, under 510(k) number K183671.
Who is the listed applicant for LG PRA.L DERMA LED MASK?
The FDA 510(k) record lists Lg Electronics.Inc as the applicant. This does not by itself establish the device manufacturer.
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.
Other records listing Lg Electronics.Inc as applicant
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: OHS)
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.