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FDA 510(k)

Upper Arm Electronic Blood Pressure Monitor

K-Number: K202372 · 2020-12-30

Decision Date2020-12-30
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Upper Arm Electronic Blood Pressure Monitor is a medical device manufactured by Conmo Electronic Company Limited. It received FDA 510(k) clearance on 2020-12-30 under approval number K202372. 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 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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.