Avazzia
K-Number: K162392 · 2017-05-12
Device Summary
Frequently Asked Questions
What is the Avazzia?
Avazzia is a medical device that received FDA 510(k) clearance on 2017-05-12. The listed applicant is Avazzia, Inc.. The 510(k) number is K162392.
When did Avazzia receive FDA 510(k) clearance?
Avazzia received FDA 510(k) clearance on 2017-05-12, under 510(k) number K162392.
Who is the listed applicant for Avazzia?
The FDA 510(k) record lists Avazzia, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Avazzia?
The FDA product code for Avazzia is NUH.
Other records listing Avazzia, 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: NUH)
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.