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FDA 510(k)

Full Automatic(NIBP) Blood Pressure Monitor

K-Number: K180240 · 2018-10-17

Decision Date2018-10-17
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Full Automatic(NIBP) Blood Pressure Monitor is the device name listed in this FDA 510(k) record. The listed applicant is Health & Life Co., Ltd.. It received FDA 510(k) clearance on 2018-10-17 under 510(k) number K180240. 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 Full Automatic(NIBP) Blood Pressure Monitor?

Full Automatic(NIBP) Blood Pressure Monitor is a medical device that received FDA 510(k) clearance on 2018-10-17. The listed applicant is Health & Life Co., Ltd.. The 510(k) number is K180240.

When did Full Automatic(NIBP) Blood Pressure Monitor receive FDA 510(k) clearance?

Full Automatic(NIBP) Blood Pressure Monitor received FDA 510(k) clearance on 2018-10-17, under 510(k) number K180240.

Who is the listed applicant for Full Automatic(NIBP) Blood Pressure Monitor?

The FDA 510(k) record lists Health & Life Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Full Automatic(NIBP) Blood Pressure Monitor?

The FDA product code for Full Automatic(NIBP) 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 Health & Life Co., Ltd. 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.

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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.