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FDA 510(k)

CARBON DIOXIDE FLOWTHROUGH LASER MIXTURES

K-Number: K904162 · 1990-10-19

ApplicantNorco, Inc.
Decision Date1990-10-19
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CARBON DIOXIDE FLOWTHROUGH LASER MIXTURES is the device name listed in this FDA 510(k) record. The listed applicant is Norco, Inc.. It received FDA 510(k) clearance on 1990-10-19 under 510(k) number K904162. 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 CARBON DIOXIDE FLOWTHROUGH LASER MIXTURES?

CARBON DIOXIDE FLOWTHROUGH LASER MIXTURES is a medical device that received FDA 510(k) clearance on 1990-10-19. The listed applicant is Norco, Inc.. The 510(k) number is K904162.

When did CARBON DIOXIDE FLOWTHROUGH LASER MIXTURES receive FDA 510(k) clearance?

CARBON DIOXIDE FLOWTHROUGH LASER MIXTURES received FDA 510(k) clearance on 1990-10-19, under 510(k) number K904162.

Who is the listed applicant for CARBON DIOXIDE FLOWTHROUGH LASER MIXTURES?

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

What is the FDA product code for CARBON DIOXIDE FLOWTHROUGH LASER MIXTURES?

The FDA product code for CARBON DIOXIDE FLOWTHROUGH LASER MIXTURES is GEX. This falls under the Gastroenterology category.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Norco, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: GEX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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