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FDA 510(k)

Electrode Pad

K-Number: K241512 · 2025-01-15

ApplicantShenzhen Deliduo Medical Technology Co.,Ltd
Decision Date2025-01-15
Product CodeGXY
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Electrode Pad is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Deliduo Medical Technology Co.,Ltd. It received FDA 510(k) clearance on 2025-01-15 under 510(k) number K241512. The device is classified under product code GXY. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Electrode Pad?

Electrode Pad is a medical device that received FDA 510(k) clearance on 2025-01-15. The listed applicant is Shenzhen Deliduo Medical Technology Co.,Ltd. The 510(k) number is K241512.

When did Electrode Pad receive FDA 510(k) clearance?

Electrode Pad received FDA 510(k) clearance on 2025-01-15, under 510(k) number K241512.

Who is the listed applicant for Electrode Pad?

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

What is the FDA product code for Electrode Pad?

The FDA product code for Electrode Pad is GXY.

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.

NCT07508774Simulation and Feasibility Study of Drone-Delivered AED for Out-of-Hospital Cardiac ArrestNOT_YET_RECRUITING

Related Devices (Code: GXY)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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