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FDA 510(k)

OMNIGUIDE BEAM PATH CO2 MARK III WAVEGUIDE FIBER

K-Number: K070157 · 2007-02-01

ApplicantOmniguide, Inc.
Decision Date2007-02-01
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

OMNIGUIDE BEAM PATH CO2 MARK III WAVEGUIDE FIBER is the device name listed in this FDA 510(k) record. The listed applicant is Omniguide, Inc.. It received FDA 510(k) clearance on 2007-02-01 under 510(k) number K070157. 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 OMNIGUIDE BEAM PATH CO2 MARK III WAVEGUIDE FIBER?

OMNIGUIDE BEAM PATH CO2 MARK III WAVEGUIDE FIBER is a medical device that received FDA 510(k) clearance on 2007-02-01. The listed applicant is Omniguide, Inc.. The 510(k) number is K070157.

When did OMNIGUIDE BEAM PATH CO2 MARK III WAVEGUIDE FIBER receive FDA 510(k) clearance?

OMNIGUIDE BEAM PATH CO2 MARK III WAVEGUIDE FIBER received FDA 510(k) clearance on 2007-02-01, under 510(k) number K070157.

Who is the listed applicant for OMNIGUIDE BEAM PATH CO2 MARK III WAVEGUIDE FIBER?

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

What is the FDA product code for OMNIGUIDE BEAM PATH CO2 MARK III WAVEGUIDE FIBER?

The FDA product code for OMNIGUIDE BEAM PATH CO2 MARK III WAVEGUIDE FIBER is GEX. This falls under the Gastroenterology category.

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Other records listing Omniguide, Inc. as applicant

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Related Devices (Code: GEX)

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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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