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FDA 510(k)

CLINICON WAVEGUIDE PLATFORM WITH INTERCONNECT FOR LUXAR ACCESSORIES

K-Number: K014236 · 2002-03-26

ApplicantClinicon Corp.
Decision Date2002-03-26
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CLINICON WAVEGUIDE PLATFORM WITH INTERCONNECT FOR LUXAR ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Clinicon Corp.. It received FDA 510(k) clearance on 2002-03-26 under 510(k) number K014236. The device is classified under product code GEX. It was reviewed by the SU advisory panel. Product code GEX falls under the category of Gastroenterology, which includes gastrointestinal diagnostic and therapeutic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLINICON WAVEGUIDE PLATFORM WITH INTERCONNECT FOR LUXAR ACCESSORIES?

CLINICON WAVEGUIDE PLATFORM WITH INTERCONNECT FOR LUXAR ACCESSORIES is a medical device that received FDA 510(k) clearance on 2002-03-26. The listed applicant is Clinicon Corp.. The 510(k) number is K014236.

When did CLINICON WAVEGUIDE PLATFORM WITH INTERCONNECT FOR LUXAR ACCESSORIES receive FDA 510(k) clearance?

CLINICON WAVEGUIDE PLATFORM WITH INTERCONNECT FOR LUXAR ACCESSORIES received FDA 510(k) clearance on 2002-03-26, under 510(k) number K014236.

Who is the listed applicant for CLINICON WAVEGUIDE PLATFORM WITH INTERCONNECT FOR LUXAR ACCESSORIES?

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

What is the FDA product code for CLINICON WAVEGUIDE PLATFORM WITH INTERCONNECT FOR LUXAR ACCESSORIES?

The FDA product code for CLINICON WAVEGUIDE PLATFORM WITH INTERCONNECT FOR LUXAR ACCESSORIES is GEX. This falls under the Gastroenterology category.

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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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