Upper Arm Electronic Blood Pressure Monitor
K-Number: K202372 · 2020-12-30
Device Summary
Frequently Asked Questions
What is the Upper Arm Electronic Blood Pressure Monitor?
Upper Arm Electronic Blood Pressure Monitor is a medical device that received FDA 510(k) clearance on 2020-12-30. It is manufactured by Conmo Electronic Company Limited. The 510(k) number is K202372.
When was Upper Arm Electronic Blood Pressure Monitor approved by the FDA?
Upper Arm Electronic Blood Pressure Monitor received FDA 510(k) clearance on 2020-12-30, under approval number K202372.
What company makes Upper Arm Electronic Blood Pressure Monitor?
Upper Arm Electronic Blood Pressure Monitor is manufactured by Conmo Electronic Company Limited.
What is the FDA product code for Upper Arm Electronic Blood Pressure Monitor?
The FDA product code for Upper Arm Electronic Blood Pressure Monitor is DXN.
Related Clinical Trials
Related PubMed Literature
Other Devices by Conmo Electronic Company Limited
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.