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FDA 510(k)

ELECTROSURGICAL DISPERSIVE ELECTRODE

K-Number: K983782 · 1999-01-25

ApplicantConmedcorp
Decision Date1999-01-25
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ELECTROSURGICAL DISPERSIVE ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Conmedcorp. It received FDA 510(k) clearance on 1999-01-25 under 510(k) number K983782. 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 DISPERSIVE ELECTRODE?

ELECTROSURGICAL DISPERSIVE ELECTRODE is a medical device that received FDA 510(k) clearance on 1999-01-25. The listed applicant is Conmedcorp. The 510(k) number is K983782.

When did ELECTROSURGICAL DISPERSIVE ELECTRODE receive FDA 510(k) clearance?

ELECTROSURGICAL DISPERSIVE ELECTRODE received FDA 510(k) clearance on 1999-01-25, under 510(k) number K983782.

Who is the listed applicant for ELECTROSURGICAL DISPERSIVE ELECTRODE?

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

What is the FDA product code for ELECTROSURGICAL DISPERSIVE ELECTRODE?

The FDA product code for ELECTROSURGICAL DISPERSIVE ELECTRODE is 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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