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FDA 510(k)

OMNIGUIDE BEAMPATH CO2 MARK I LASER BEAM DELIVERY

K-Number: K050541 · 2005-05-09

ApplicantOmniguide Communications, Inc.
Decision Date2005-05-09
Product CodeHQF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

OMNIGUIDE BEAMPATH CO2 MARK I LASER BEAM DELIVERY is the device name listed in this FDA 510(k) record. The listed applicant is Omniguide Communications, Inc.. It received FDA 510(k) clearance on 2005-05-09 under 510(k) number K050541. The device is classified under product code HQF. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OMNIGUIDE BEAMPATH CO2 MARK I LASER BEAM DELIVERY?

OMNIGUIDE BEAMPATH CO2 MARK I LASER BEAM DELIVERY is a medical device that received FDA 510(k) clearance on 2005-05-09. The listed applicant is Omniguide Communications, Inc.. The 510(k) number is K050541.

When did OMNIGUIDE BEAMPATH CO2 MARK I LASER BEAM DELIVERY receive FDA 510(k) clearance?

OMNIGUIDE BEAMPATH CO2 MARK I LASER BEAM DELIVERY received FDA 510(k) clearance on 2005-05-09, under 510(k) number K050541.

Who is the listed applicant for OMNIGUIDE BEAMPATH CO2 MARK I LASER BEAM DELIVERY?

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

What is the FDA product code for OMNIGUIDE BEAMPATH CO2 MARK I LASER BEAM DELIVERY?

The FDA product code for OMNIGUIDE BEAMPATH CO2 MARK I LASER BEAM DELIVERY is HQF.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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