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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 the device name listed in this FDA 510(k) record. The listed applicant is Conmo Electronic Company Limited. It received FDA 510(k) clearance on 2020-12-30 under 510(k) 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. The listed applicant is Conmo Electronic Company Limited. The 510(k) number is K202372.

When did Upper Arm Electronic Blood Pressure Monitor receive FDA 510(k) clearance?

Upper Arm Electronic Blood Pressure Monitor received FDA 510(k) clearance on 2020-12-30, under 510(k) number K202372.

Who is the listed applicant for Upper Arm Electronic Blood Pressure Monitor?

The FDA 510(k) record lists Conmo Electronic Company Limited as the applicant. This does not by itself establish the device manufacturer.

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 records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Conmo Electronic Company Limited as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: DXN)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.