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FDA 510(k)

CONDUCTIVE ADHESIVE DISPERSIVE ELECTRO

K-Number: K822405 · 1982-09-21

ApplicantEdward Weck, Inc.
Decision Date1982-09-21
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CONDUCTIVE ADHESIVE DISPERSIVE ELECTRO is the device name listed in this FDA 510(k) record. The listed applicant is Edward Weck, Inc.. It received FDA 510(k) clearance on 1982-09-21 under 510(k) number K822405. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONDUCTIVE ADHESIVE DISPERSIVE ELECTRO?

CONDUCTIVE ADHESIVE DISPERSIVE ELECTRO is a medical device that received FDA 510(k) clearance on 1982-09-21. The listed applicant is Edward Weck, Inc.. The 510(k) number is K822405.

When did CONDUCTIVE ADHESIVE DISPERSIVE ELECTRO receive FDA 510(k) clearance?

CONDUCTIVE ADHESIVE DISPERSIVE ELECTRO received FDA 510(k) clearance on 1982-09-21, under 510(k) number K822405.

Who is the listed applicant for CONDUCTIVE ADHESIVE DISPERSIVE ELECTRO?

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

What is the FDA product code for CONDUCTIVE ADHESIVE DISPERSIVE ELECTRO?

The FDA product code for CONDUCTIVE ADHESIVE DISPERSIVE ELECTRO is GEI.

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Other records listing Edward Weck, Inc. as applicant

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Related Devices (Code: GEI)

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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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