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)

U80 Series Upper Arm Electronic Blood Pressure Monitor

K-Number: K160019 · 2016-04-22

Decision Date2016-04-22
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

U80 Series Upper Arm Electronic Blood Pressure Monitor is a medical device manufactured by Shenzhen Urion Technology Co., Ltd.. It received FDA 510(k) clearance on 2016-04-22 under approval number K160019. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the U80 Series Upper Arm Electronic Blood Pressure Monitor?

U80 Series Upper Arm Electronic Blood Pressure Monitor is a medical device that received FDA 510(k) clearance on 2016-04-22. It is manufactured by Shenzhen Urion Technology Co., Ltd.. The 510(k) number is K160019.

When was U80 Series Upper Arm Electronic Blood Pressure Monitor approved by the FDA?

U80 Series Upper Arm Electronic Blood Pressure Monitor received FDA 510(k) clearance on 2016-04-22, under approval number K160019.

What company makes U80 Series Upper Arm Electronic Blood Pressure Monitor?

U80 Series Upper Arm Electronic Blood Pressure Monitor is manufactured by Shenzhen Urion Technology Co., Ltd..

What is the FDA product code for U80 Series Upper Arm Electronic Blood Pressure Monitor?

The FDA product code for U80 Series Upper Arm Electronic Blood Pressure Monitor is DXN.

Related Clinical Trials

Related PubMed Literature

Other Devices by Shenzhen Urion Technology Co., Ltd.

View all 7 devices →

Related Devices (Code: DXN)

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.