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FDA 510(k)

ELECTRONIC BLOOD PRESSURE MONITOR FOR UPPER ARM

K-Number: K130232 · 2013-09-17

Decision Date2013-09-17
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ELECTRONIC BLOOD PRESSURE MONITOR FOR UPPER ARM is the device name listed in this FDA 510(k) record. The listed applicant is Jinxinbao Electronic Co.,Ltd. It received FDA 510(k) clearance on 2013-09-17 under 510(k) number K130232. 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 ELECTRONIC BLOOD PRESSURE MONITOR FOR UPPER ARM?

ELECTRONIC BLOOD PRESSURE MONITOR FOR UPPER ARM is a medical device that received FDA 510(k) clearance on 2013-09-17. The listed applicant is Jinxinbao Electronic Co.,Ltd. The 510(k) number is K130232.

When did ELECTRONIC BLOOD PRESSURE MONITOR FOR UPPER ARM receive FDA 510(k) clearance?

ELECTRONIC BLOOD PRESSURE MONITOR FOR UPPER ARM received FDA 510(k) clearance on 2013-09-17, under 510(k) number K130232.

Who is the listed applicant for ELECTRONIC BLOOD PRESSURE MONITOR FOR UPPER ARM?

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

What is the FDA product code for ELECTRONIC BLOOD PRESSURE MONITOR FOR UPPER ARM?

The FDA product code for ELECTRONIC BLOOD PRESSURE MONITOR FOR UPPER ARM 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 Jinxinbao Electronic 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.

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.

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