Electronic Blood Pressure Monitor
K-Number: K191180 · 2019-08-23
Device Summary
Frequently Asked Questions
What is the Electronic Blood Pressure Monitor?
Electronic Blood Pressure Monitor is a medical device that received FDA 510(k) clearance on 2019-08-23. It is manufactured by Shenzhen AOJ Medical Technology Co., Ltd.. The 510(k) number is K191180.
When was Electronic Blood Pressure Monitor approved by the FDA?
Electronic Blood Pressure Monitor received FDA 510(k) clearance on 2019-08-23, under approval number K191180.
What company makes Electronic Blood Pressure Monitor?
Electronic Blood Pressure Monitor is manufactured by Shenzhen AOJ Medical Technology Co., Ltd..
What is the FDA product code for Electronic Blood Pressure Monitor?
The FDA product code for Electronic Blood Pressure Monitor is DXN.
Related Clinical Trials
Related PubMed Literature
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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.