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FDA 510(k)

LIFECARE CONDUCTIVE GARMENTS

K-Number: K103719 · 2011-08-24

Decision Date2011-08-24
Product CodeGXY
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

LIFECARE CONDUCTIVE GARMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Everyway Medical Instruments Co.,Ltd. It received FDA 510(k) clearance on 2011-08-24 under 510(k) number K103719. 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 LIFECARE CONDUCTIVE GARMENTS?

LIFECARE CONDUCTIVE GARMENTS is a medical device that received FDA 510(k) clearance on 2011-08-24. The listed applicant is Everyway Medical Instruments Co.,Ltd. The 510(k) number is K103719.

When did LIFECARE CONDUCTIVE GARMENTS receive FDA 510(k) clearance?

LIFECARE CONDUCTIVE GARMENTS received FDA 510(k) clearance on 2011-08-24, under 510(k) number K103719.

Who is the listed applicant for LIFECARE CONDUCTIVE GARMENTS?

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

What is the FDA product code for LIFECARE CONDUCTIVE GARMENTS?

The FDA product code for LIFECARE CONDUCTIVE GARMENTS 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 Everyway Medical Instruments 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 27 devices →

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

View on FDA Database →

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

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