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FDA 510(k)

CONMED GOLDVAC INTEGRATED SMOKE EVACUATION PENCIL

K-Number: K081634 · 2008-06-25

ApplicantConmed Corporation
Decision Date2008-06-25
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CONMED GOLDVAC INTEGRATED SMOKE EVACUATION PENCIL is the device name listed in this FDA 510(k) record. The listed applicant is Conmed Corporation. It received FDA 510(k) clearance on 2008-06-25 under 510(k) number K081634. 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 GOLDVAC INTEGRATED SMOKE EVACUATION PENCIL?

CONMED GOLDVAC INTEGRATED SMOKE EVACUATION PENCIL is a medical device that received FDA 510(k) clearance on 2008-06-25. The listed applicant is Conmed Corporation. The 510(k) number is K081634.

When did CONMED GOLDVAC INTEGRATED SMOKE EVACUATION PENCIL receive FDA 510(k) clearance?

CONMED GOLDVAC INTEGRATED SMOKE EVACUATION PENCIL received FDA 510(k) clearance on 2008-06-25, under 510(k) number K081634.

Who is the listed applicant for CONMED GOLDVAC INTEGRATED SMOKE EVACUATION PENCIL?

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 GOLDVAC INTEGRATED SMOKE EVACUATION PENCIL?

The FDA product code for CONMED GOLDVAC INTEGRATED SMOKE EVACUATION PENCIL 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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