K800078Substantially Equivalent

Briox Model-Aeromist

Name: K800078 Briox Model-Aeromist
Creator: Briox Technologies, Inc.
Published: 1980-02-05
License: https://open.fda.gov/license/

Briox Technologies, Inc., Mchenry IL / Traditional, Substantially Equivalent

FDA source

K800078 is the FDA 510(k) clearance record for BRIOX MODEL-AEROMIST, cleared for Briox Technologies, Inc. on 1980-02-05. FDA records list 6 510(k) clearances for Briox Technologies, Inc., from 1979-07-24 to 1982-01-12. As of 2026-09-10, FDA records show no recalls naming K800078.

Clearance record

Decision date: 1980-02-05
Received: 1980-01-14 (22 days to decision)
Review panel: Unknown
Applicant: Briox Technologies, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review: No