FDA 510(k)

ELECTROSURGICAL AND ARTHROSCOPY ACCESSORY ELECTRODES

K-Number: K961812 · 1996-06-13

Decision Date1996-06-13

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

ELECTROSURGICAL AND ARTHROSCOPY ACCESSORY ELECTRODES is the device name listed in this FDA 510(k) record. The listed applicant is Conmedcorp. It received FDA 510(k) clearance on 1996-06-13 under 510(k) number K961812. 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 AND ARTHROSCOPY ACCESSORY ELECTRODES?

ELECTROSURGICAL AND ARTHROSCOPY ACCESSORY ELECTRODES is a medical device that received FDA 510(k) clearance on 1996-06-13. The listed applicant is Conmedcorp. The 510(k) number is K961812.

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

ELECTROSURGICAL AND ARTHROSCOPY ACCESSORY ELECTRODES received FDA 510(k) clearance on 1996-06-13, under 510(k) number K961812.

Who is the listed applicant for ELECTROSURGICAL AND ARTHROSCOPY ACCESSORY ELECTRODES?

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 AND ARTHROSCOPY ACCESSORY ELECTRODES?

The FDA product code for ELECTROSURGICAL AND ARTHROSCOPY ACCESSORY ELECTRODES is GEI.

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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.