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FDA 510(k)

CONDUCTIVITY GEL W/POTASSIUM CHLORIDE

K-Number: K770622 · 1977-04-07

Decision Date1977-04-07
Product CodeGYB
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

CONDUCTIVITY GEL W/POTASSIUM CHLORIDE is the device name listed in this FDA 510(k) record. The listed applicant is Graphic Controls Corp.. It received FDA 510(k) clearance on 1977-04-07 under 510(k) number K770622. 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 CONDUCTIVITY GEL W/POTASSIUM CHLORIDE?

CONDUCTIVITY GEL W/POTASSIUM CHLORIDE is a medical device that received FDA 510(k) clearance on 1977-04-07. The listed applicant is Graphic Controls Corp.. The 510(k) number is K770622.

When did CONDUCTIVITY GEL W/POTASSIUM CHLORIDE receive FDA 510(k) clearance?

CONDUCTIVITY GEL W/POTASSIUM CHLORIDE received FDA 510(k) clearance on 1977-04-07, under 510(k) number K770622.

Who is the listed applicant for CONDUCTIVITY GEL W/POTASSIUM CHLORIDE?

The FDA 510(k) record lists Graphic Controls Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CONDUCTIVITY GEL W/POTASSIUM CHLORIDE?

The FDA product code for CONDUCTIVITY GEL W/POTASSIUM CHLORIDE 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 Graphic Controls Corp. 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 55 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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