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FDA 510(k)

CONMED HEATWAVE HAND-CONTROLLED ELETRODE

K-Number: K021299 · 2002-06-26

ApplicantConmedcorp
Decision Date2002-06-26
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CONMED HEATWAVE HAND-CONTROLLED ELETRODE is the device name listed in this FDA 510(k) record. The listed applicant is Conmedcorp. It received FDA 510(k) clearance on 2002-06-26 under 510(k) number K021299. 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 CONMED HEATWAVE HAND-CONTROLLED ELETRODE?

CONMED HEATWAVE HAND-CONTROLLED ELETRODE is a medical device that received FDA 510(k) clearance on 2002-06-26. The listed applicant is Conmedcorp. The 510(k) number is K021299.

When did CONMED HEATWAVE HAND-CONTROLLED ELETRODE receive FDA 510(k) clearance?

CONMED HEATWAVE HAND-CONTROLLED ELETRODE received FDA 510(k) clearance on 2002-06-26, under 510(k) number K021299.

Who is the listed applicant for CONMED HEATWAVE HAND-CONTROLLED ELETRODE?

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 CONMED HEATWAVE HAND-CONTROLLED ELETRODE?

The FDA product code for CONMED HEATWAVE HAND-CONTROLLED ELETRODE is GEI.

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Related Devices (Code: 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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