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FDA 510(k)

CONMED SYSTEM 5000 ESU

K-Number: K020186 · 2002-04-12

ApplicantConmedcorp
Decision Date2002-04-12
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CONMED SYSTEM 5000 ESU is the device name listed in this FDA 510(k) record. The listed applicant is Conmedcorp. It received FDA 510(k) clearance on 2002-04-12 under 510(k) number K020186. 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 5000 ESU?

CONMED SYSTEM 5000 ESU is a medical device that received FDA 510(k) clearance on 2002-04-12. The listed applicant is Conmedcorp. The 510(k) number is K020186.

When did CONMED SYSTEM 5000 ESU receive FDA 510(k) clearance?

CONMED SYSTEM 5000 ESU received FDA 510(k) clearance on 2002-04-12, under 510(k) number K020186.

Who is the listed applicant for CONMED SYSTEM 5000 ESU?

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 SYSTEM 5000 ESU?

The FDA product code for CONMED SYSTEM 5000 ESU 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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