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FDA 510(k)

Conductive Gel

K-Number: K222770 · 2022-12-13

Decision Date2022-12-13
Product CodeGYB
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Conductive Gel is the device name listed in this FDA 510(k) record. The listed applicant is Top-Rank Health Care Co., Ltd.. It received FDA 510(k) clearance on 2022-12-13 under 510(k) number K222770. 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 Conductive Gel?

Conductive Gel is a medical device that received FDA 510(k) clearance on 2022-12-13. The listed applicant is Top-Rank Health Care Co., Ltd.. The 510(k) number is K222770.

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

Conductive Gel received FDA 510(k) clearance on 2022-12-13, under 510(k) number K222770.

Who is the listed applicant for Conductive Gel?

The FDA 510(k) record lists Top-Rank Health Care Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Conductive Gel?

The FDA product code for Conductive Gel is GYB.

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 Top-Rank Health Care 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.

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

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