Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Zia

K-Number: K160852 · 2016-12-15

ApplicantZetta Medical Technologies, LLC
Decision Date2016-12-15
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Zia is a medical device manufactured by Zetta Medical Technologies, LLC. It received FDA 510(k) clearance on 2016-12-15 under approval number K160852. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Zia?

Zia is a medical device that received FDA 510(k) clearance on 2016-12-15. It is manufactured by Zetta Medical Technologies, LLC. The 510(k) number is K160852.

When was Zia approved by the FDA?

Zia received FDA 510(k) clearance on 2016-12-15, under approval number K160852.

What company makes Zia?

Zia is manufactured by Zetta Medical Technologies, LLC.

What is the FDA product code for Zia?

The FDA product code for Zia is LLZ.

Other Devices by Zetta Medical Technologies, LLC

K170273Z-DOSE29 K172768ZOOM

Related Devices (Code: LLZ)

K161959ClearView cCADClearview Diagnostics, Inc. K163539Ez3D-i / E3Ewoosoft Co., Ltd. K162955Multi-Modality Tumor Tracking (MMTT) applicationPhilips Medical Systems Nederland B.V. K162376CAAS MR 4D FlowPie Medical Imaging BV K161322CT CoPilotZepmed, LLC K152009DENSEEMAMMO v1.0Statlife

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.

↑