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FDA 510(k)

TEN-20 CONDUCTIVE PASTE GEL

K-Number: K933799 · 1994-05-27

Decision Date1994-05-27
Product CodeGYB
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

TEN-20 CONDUCTIVE PASTE 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 1994-05-27 under 510(k) number K933799. 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 TEN-20 CONDUCTIVE PASTE GEL?

TEN-20 CONDUCTIVE PASTE GEL is a medical device that received FDA 510(k) clearance on 1994-05-27. The listed applicant is Cadwell Laboratories, Inc.. The 510(k) number is K933799.

When did TEN-20 CONDUCTIVE PASTE GEL receive FDA 510(k) clearance?

TEN-20 CONDUCTIVE PASTE GEL received FDA 510(k) clearance on 1994-05-27, under 510(k) number K933799.

Who is the listed applicant for TEN-20 CONDUCTIVE PASTE 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 TEN-20 CONDUCTIVE PASTE GEL?

The FDA product code for TEN-20 CONDUCTIVE PASTE GEL is GYB.

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 Cadwell Laboratories, 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 46 devices →

Related Devices (Code: GYB)

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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