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FDA 510(k)

Arm Blood Pressure Monitor

K-Number: K180435 · 2019-01-03

Decision Date2019-01-03
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Arm Blood Pressure Monitor is a medical device manufactured by Alicn Medical (Shenzhen), Inc.. It received FDA 510(k) clearance on 2019-01-03 under approval number K180435. 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 Arm Blood Pressure Monitor?

Arm Blood Pressure Monitor is a medical device that received FDA 510(k) clearance on 2019-01-03. It is manufactured by Alicn Medical (Shenzhen), Inc.. The 510(k) number is K180435.

When was Arm Blood Pressure Monitor approved by the FDA?

Arm Blood Pressure Monitor received FDA 510(k) clearance on 2019-01-03, under approval number K180435.

What company makes Arm Blood Pressure Monitor?

Arm Blood Pressure Monitor is manufactured by Alicn Medical (Shenzhen), Inc..

What is the FDA product code for Arm Blood Pressure Monitor?

The FDA product code for Arm Blood Pressure Monitor is DXN.

Related Clinical Trials

Related PubMed Literature

Other Devices by Alicn Medical (Shenzhen), Inc.

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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.