Zia
K-Number: K160852 · 2016-12-15
Device Summary
Frequently Asked Questions
What is the Zia?
Zia is a medical device that received FDA 510(k) clearance on 2016-12-15. The listed applicant is Zetta Medical Technologies, LLC. The 510(k) number is K160852.
When did Zia receive FDA 510(k) clearance?
Zia received FDA 510(k) clearance on 2016-12-15, under 510(k) number K160852.
Who is the listed applicant for Zia?
The FDA 510(k) record lists Zetta Medical Technologies, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Zia?
The FDA product code for Zia is LLZ.
Other records listing Zetta Medical Technologies, LLC 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: LLZ)
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.