Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Red Light Hair Growth Cap (LP-RJVGRW-BLK)

K-Number: K250467 · 2025-06-05

Decision Date2025-06-05
Product CodeOAP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Red Light Hair Growth Cap (LP-RJVGRW-BLK) is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Idea Light Limited. It received FDA 510(k) clearance on 2025-06-05 under 510(k) number K250467. 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 Red Light Hair Growth Cap (LP-RJVGRW-BLK)?

Red Light Hair Growth Cap (LP-RJVGRW-BLK) is a medical device that received FDA 510(k) clearance on 2025-06-05. The listed applicant is Shenzhen Idea Light Limited. The 510(k) number is K250467.

When did Red Light Hair Growth Cap (LP-RJVGRW-BLK) receive FDA 510(k) clearance?

Red Light Hair Growth Cap (LP-RJVGRW-BLK) received FDA 510(k) clearance on 2025-06-05, under 510(k) number K250467.

Who is the listed applicant for Red Light Hair Growth Cap (LP-RJVGRW-BLK)?

The FDA 510(k) record lists Shenzhen Idea Light Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Red Light Hair Growth Cap (LP-RJVGRW-BLK)?

The FDA product code for Red Light Hair Growth Cap (LP-RJVGRW-BLK) is OAP.

Related Clinical Trials

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.

Other records listing Shenzhen Idea Light Limited 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: OAP)

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.