FDA 510(k)

LG Pra. L Derma LD Scalp Care

K-Number: K200464 · 2020-07-23

Decision Date2020-07-23

Product CodeOAP

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

LG Pra. L Derma LD Scalp Care is a medical device manufactured by Lg Electronics.Inc. It received FDA 510(k) clearance on 2020-07-23 under approval number K200464. The device is classified under product code OAP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LG Pra. L Derma LD Scalp Care?

LG Pra. L Derma LD Scalp Care is a medical device that received FDA 510(k) clearance on 2020-07-23. It is manufactured by Lg Electronics.Inc. The 510(k) number is K200464.

When was LG Pra. L Derma LD Scalp Care approved by the FDA?

LG Pra. L Derma LD Scalp Care received FDA 510(k) clearance on 2020-07-23, under approval number K200464.

What company makes LG Pra. L Derma LD Scalp Care?

LG Pra. L Derma LD Scalp Care is manufactured by Lg Electronics.Inc.

What is the FDA product code for LG Pra. L Derma LD Scalp Care?

The FDA product code for LG Pra. L Derma LD Scalp Care is OAP.

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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.