Wrist Type Automatic Blood Pressure Monitor
K-Number: K172972 · 2018-03-02
Device Summary
Frequently Asked Questions
What is the Wrist Type Automatic Blood Pressure Monitor?
Wrist Type Automatic Blood Pressure Monitor is a medical device that received FDA 510(k) clearance on 2018-03-02. It is manufactured by Shenzhen Jiacom Technology CO ., Ltd.. The 510(k) number is K172972.
When was Wrist Type Automatic Blood Pressure Monitor approved by the FDA?
Wrist Type Automatic Blood Pressure Monitor received FDA 510(k) clearance on 2018-03-02, under approval number K172972.
What company makes Wrist Type Automatic Blood Pressure Monitor?
Wrist Type Automatic Blood Pressure Monitor is manufactured by Shenzhen Jiacom Technology CO ., Ltd..
What is the FDA product code for Wrist Type Automatic Blood Pressure Monitor?
The FDA product code for Wrist Type Automatic 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.