Wrist Blood Pressure Monitor, Blood Pressure Monitor
K-Number: K210768 · 2021-07-30
Device Summary
Frequently Asked Questions
What is the Wrist Blood Pressure Monitor, Blood Pressure Monitor?
Wrist Blood Pressure Monitor, Blood Pressure Monitor is a medical device that received FDA 510(k) clearance on 2021-07-30. It is manufactured by Andon Health Co, Ltd.. The 510(k) number is K210768.
When was Wrist Blood Pressure Monitor, Blood Pressure Monitor approved by the FDA?
Wrist Blood Pressure Monitor, Blood Pressure Monitor received FDA 510(k) clearance on 2021-07-30, under approval number K210768.
What company makes Wrist Blood Pressure Monitor, Blood Pressure Monitor?
Wrist Blood Pressure Monitor, Blood Pressure Monitor is manufactured by Andon Health Co, Ltd..
What is the FDA product code for Wrist Blood Pressure Monitor, Blood Pressure Monitor?
The FDA product code for Wrist Blood Pressure Monitor, 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.