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FDA 510(k)

BEAMER ARGON PROBE

K-Number: K081644 · 2008-09-10

ApplicantConmed Corporation
Decision Date2008-09-10
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BEAMER ARGON PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Conmed Corporation. It received FDA 510(k) clearance on 2008-09-10 under 510(k) number K081644. 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 BEAMER ARGON PROBE?

BEAMER ARGON PROBE is a medical device that received FDA 510(k) clearance on 2008-09-10. The listed applicant is Conmed Corporation. The 510(k) number is K081644.

When did BEAMER ARGON PROBE receive FDA 510(k) clearance?

BEAMER ARGON PROBE received FDA 510(k) clearance on 2008-09-10, under 510(k) number K081644.

Who is the listed applicant for BEAMER ARGON PROBE?

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 BEAMER ARGON PROBE?

The FDA product code for BEAMER ARGON PROBE 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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