FDA 510(k)

BRIOX MODEL-AEROMIST

K-Number: K800078 · 1980-02-05

Decision Date1980-02-05

Product Code

DecisionSubstantially Equivalent

Device Summary

BRIOX MODEL-AEROMIST 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 1980-02-05 under 510(k) number K800078. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BRIOX MODEL-AEROMIST?

BRIOX MODEL-AEROMIST is a medical device that received FDA 510(k) clearance on 1980-02-05. The listed applicant is Briox Technologies, Inc.. The 510(k) number is K800078.

When did BRIOX MODEL-AEROMIST receive FDA 510(k) clearance?

BRIOX MODEL-AEROMIST received FDA 510(k) clearance on 1980-02-05, under 510(k) number K800078.

Who is the listed applicant for BRIOX MODEL-AEROMIST?

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

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Other records listing Briox Technologies, Inc. as applicant

K813507INFALERT K791240BRIOX MODEL 2000-C COMPRESSOR UNIT K791238BRIOX MODEL 2000-CQ QUIET COMPRESSOR K791239BRIOX MODEL 2000-A ASPIRATOR UNIT K791241BRIOX MODEL 2000-CA COMPRESSOR UNIT

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.