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FDA 510(k)

Wrist Blood Pressure Monitor, Blood Pressure Monitor

K-Number: K210768 · 2021-07-30

Decision Date2021-07-30
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Wrist Blood Pressure Monitor, Blood Pressure Monitor is a medical device manufactured by Andon Health Co, Ltd.. It received FDA 510(k) clearance on 2021-07-30 under approval number K210768. 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 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.

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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.