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)

Jmoon Conductive Gel

K-Number: K243749 · 2025-04-08

Decision Date2025-04-08
Product CodeGYB
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Jmoon Conductive Gel is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Ulike Smart Electronics Co., Ltd.. It received FDA 510(k) clearance on 2025-04-08 under 510(k) number K243749. The device is classified under product code GYB. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Jmoon Conductive Gel?

Jmoon Conductive Gel is a medical device that received FDA 510(k) clearance on 2025-04-08. The listed applicant is Shenzhen Ulike Smart Electronics Co., Ltd.. The 510(k) number is K243749.

When did Jmoon Conductive Gel receive FDA 510(k) clearance?

Jmoon Conductive Gel received FDA 510(k) clearance on 2025-04-08, under 510(k) number K243749.

Who is the listed applicant for Jmoon Conductive Gel?

The FDA 510(k) record lists Shenzhen Ulike Smart Electronics Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Jmoon Conductive Gel?

The FDA product code for Jmoon Conductive Gel is GYB.

Other records listing Shenzhen Ulike Smart Electronics Co., Ltd. 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.

View all 23 devices →

Related Devices (Code: GYB)

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.