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FDA 510(k)

LG Pra. L Derma LD Scalp Care

K-Number: K200464 · 2020-07-23

ApplicantLg Electronics.Inc
Decision Date2020-07-23
Product CodeOAP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

LG Pra. L Derma LD Scalp Care is the device name listed in this FDA 510(k) record. The listed applicant is Lg Electronics.Inc. It received FDA 510(k) clearance on 2020-07-23 under 510(k) 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. The listed applicant is Lg Electronics.Inc. The 510(k) number is K200464.

When did LG Pra. L Derma LD Scalp Care receive FDA 510(k) clearance?

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

Who is the listed applicant for LG Pra. L Derma LD Scalp Care?

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 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.

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