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FDA 510(k)

DISPOS. CONDUCTIVE ADHESIVE TENS PAD

K-Number: K850311 · 1985-03-05

Decision Date1985-03-05
Product CodeGXY
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

DISPOS. CONDUCTIVE ADHESIVE TENS PAD is the device name listed in this FDA 510(k) record. The listed applicant is Consolidated Medical Equipment, Inc.. It received FDA 510(k) clearance on 1985-03-05 under 510(k) number K850311. 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 DISPOS. CONDUCTIVE ADHESIVE TENS PAD?

DISPOS. CONDUCTIVE ADHESIVE TENS PAD is a medical device that received FDA 510(k) clearance on 1985-03-05. The listed applicant is Consolidated Medical Equipment, Inc.. The 510(k) number is K850311.

When did DISPOS. CONDUCTIVE ADHESIVE TENS PAD receive FDA 510(k) clearance?

DISPOS. CONDUCTIVE ADHESIVE TENS PAD received FDA 510(k) clearance on 1985-03-05, under 510(k) number K850311.

Who is the listed applicant for DISPOS. CONDUCTIVE ADHESIVE TENS PAD?

The FDA 510(k) record lists Consolidated Medical Equipment, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DISPOS. CONDUCTIVE ADHESIVE TENS PAD?

The FDA product code for DISPOS. CONDUCTIVE ADHESIVE TENS 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.

Other records listing Consolidated Medical Equipment, Inc. 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 15 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

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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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