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FDA 510(k)

ELECTROSURGICAL ELECTRODES

K-Number: K923332 · 1992-10-13

Decision Date1992-10-13
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ELECTROSURGICAL ELECTRODES is the device name listed in this FDA 510(k) record. The listed applicant is Premier Dental Products Co.. It received FDA 510(k) clearance on 1992-10-13 under 510(k) number K923332. 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 ELECTROSURGICAL ELECTRODES?

ELECTROSURGICAL ELECTRODES is a medical device that received FDA 510(k) clearance on 1992-10-13. The listed applicant is Premier Dental Products Co.. The 510(k) number is K923332.

When did ELECTROSURGICAL ELECTRODES receive FDA 510(k) clearance?

ELECTROSURGICAL ELECTRODES received FDA 510(k) clearance on 1992-10-13, under 510(k) number K923332.

Who is the listed applicant for ELECTROSURGICAL ELECTRODES?

The FDA 510(k) record lists Premier Dental Products Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELECTROSURGICAL ELECTRODES?

The FDA product code for ELECTROSURGICAL ELECTRODES is GEI.

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 Premier Dental Products Co. 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 40 devices →

Related Devices (Code: GEI)

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

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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