FDA 510(k)

CONMED SYSTEM MODEL 2450 ELECTROSURGICAL GENERATOR

K-Number: K052009 · 2005-09-28

Decision Date2005-09-28

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

CONMED SYSTEM MODEL 2450 ELECTROSURGICAL GENERATOR is the device name listed in this FDA 510(k) record. The listed applicant is Conmed Corporation. It received FDA 510(k) clearance on 2005-09-28 under 510(k) number K052009. 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 SYSTEM MODEL 2450 ELECTROSURGICAL GENERATOR?

CONMED SYSTEM MODEL 2450 ELECTROSURGICAL GENERATOR is a medical device that received FDA 510(k) clearance on 2005-09-28. The listed applicant is Conmed Corporation. The 510(k) number is K052009.

When did CONMED SYSTEM MODEL 2450 ELECTROSURGICAL GENERATOR receive FDA 510(k) clearance?

CONMED SYSTEM MODEL 2450 ELECTROSURGICAL GENERATOR received FDA 510(k) clearance on 2005-09-28, under 510(k) number K052009.

Who is the listed applicant for CONMED SYSTEM MODEL 2450 ELECTROSURGICAL GENERATOR?

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

What is the FDA product code for CONMED SYSTEM MODEL 2450 ELECTROSURGICAL GENERATOR?

The FDA product code for CONMED SYSTEM MODEL 2450 ELECTROSURGICAL GENERATOR 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.