BRIOX MODEL 2000-A ASPIRATOR UNIT
K-Number: K791239 · 1979-07-24
Advertisement
Device Summary
Frequently Asked Questions
What is the BRIOX MODEL 2000-A ASPIRATOR UNIT?
BRIOX MODEL 2000-A ASPIRATOR UNIT 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 K791239.
When did BRIOX MODEL 2000-A ASPIRATOR UNIT receive FDA 510(k) clearance?
BRIOX MODEL 2000-A ASPIRATOR UNIT received FDA 510(k) clearance on 1979-07-24, under 510(k) number K791239.
Who is the listed applicant for BRIOX MODEL 2000-A ASPIRATOR UNIT?
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-A ASPIRATOR UNIT?
The FDA product code for BRIOX MODEL 2000-A ASPIRATOR UNIT 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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement