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FDA 510(k)

HOME CARE VARIOUS MODELS OF SELF-ADHESIVE ELECTRODES

K-Number: K022917 · 2003-03-04

Decision Date2003-03-04
Product CodeGXY
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

HOME CARE VARIOUS MODELS OF SELF-ADHESIVE ELECTRODES is the device name listed in this FDA 510(k) record. The listed applicant is Home Care Technology Co., Ltd.. It received FDA 510(k) clearance on 2003-03-04 under 510(k) number K022917. 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 HOME CARE VARIOUS MODELS OF SELF-ADHESIVE ELECTRODES?

HOME CARE VARIOUS MODELS OF SELF-ADHESIVE ELECTRODES is a medical device that received FDA 510(k) clearance on 2003-03-04. The listed applicant is Home Care Technology Co., Ltd.. The 510(k) number is K022917.

When did HOME CARE VARIOUS MODELS OF SELF-ADHESIVE ELECTRODES receive FDA 510(k) clearance?

HOME CARE VARIOUS MODELS OF SELF-ADHESIVE ELECTRODES received FDA 510(k) clearance on 2003-03-04, under 510(k) number K022917.

Who is the listed applicant for HOME CARE VARIOUS MODELS OF SELF-ADHESIVE ELECTRODES?

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

What is the FDA product code for HOME CARE VARIOUS MODELS OF SELF-ADHESIVE ELECTRODES?

The FDA product code for HOME CARE VARIOUS MODELS OF SELF-ADHESIVE ELECTRODES 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.

Other records listing Home Care Technology 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: GXY)

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

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