FDA 510(k)

LECTRON II CONDUCTIVE GEL/CADWELL ELECTRODE GEL

K-Number: K933804 · 1994-03-22

Decision Date1994-03-22

Product CodeGYB

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

LECTRON II CONDUCTIVE GEL/CADWELL ELECTRODE GEL is the device name listed in this FDA 510(k) record. The listed applicant is Cadwell Laboratories, Inc.. It received FDA 510(k) clearance on 1994-03-22 under 510(k) number K933804. The device is classified under product code GYB. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LECTRON II CONDUCTIVE GEL/CADWELL ELECTRODE GEL?

LECTRON II CONDUCTIVE GEL/CADWELL ELECTRODE GEL is a medical device that received FDA 510(k) clearance on 1994-03-22. The listed applicant is Cadwell Laboratories, Inc.. The 510(k) number is K933804.

When did LECTRON II CONDUCTIVE GEL/CADWELL ELECTRODE GEL receive FDA 510(k) clearance?

LECTRON II CONDUCTIVE GEL/CADWELL ELECTRODE GEL received FDA 510(k) clearance on 1994-03-22, under 510(k) number K933804.

Who is the listed applicant for LECTRON II CONDUCTIVE GEL/CADWELL ELECTRODE GEL?

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

What is the FDA product code for LECTRON II CONDUCTIVE GEL/CADWELL ELECTRODE GEL?

The FDA product code for LECTRON II CONDUCTIVE GEL/CADWELL ELECTRODE GEL is GYB.

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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.