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FDA 510(k)

BRIOX MODEL 2000-CQ QUIET COMPRESSOR

K-Number: K791238 · 1979-07-24

Decision Date1979-07-24
Product CodeJCX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BRIOX MODEL 2000-CQ QUIET COMPRESSOR is the device name listed in this FDA 510(k) record. The listed applicant is Briox Technologies, Inc.. It received FDA 510(k) clearance on 1979-07-24 under 510(k) number K791238. The device is classified under product code JCX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BRIOX MODEL 2000-CQ QUIET COMPRESSOR?

BRIOX MODEL 2000-CQ QUIET COMPRESSOR is a medical device that received FDA 510(k) clearance on 1979-07-24. The listed applicant is Briox Technologies, Inc.. The 510(k) number is K791238.

When did BRIOX MODEL 2000-CQ QUIET COMPRESSOR receive FDA 510(k) clearance?

BRIOX MODEL 2000-CQ QUIET COMPRESSOR received FDA 510(k) clearance on 1979-07-24, under 510(k) number K791238.

Who is the listed applicant for BRIOX MODEL 2000-CQ QUIET COMPRESSOR?

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

What is the FDA product code for BRIOX MODEL 2000-CQ QUIET COMPRESSOR?

The FDA product code for BRIOX MODEL 2000-CQ QUIET COMPRESSOR is JCX.

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 Briox Technologies, 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: JCX)

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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