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FDA 510(k)

BLOOD PRESSURE MONITOR WITH STETHOSCOPE

K-Number: K122259 · 2012-09-24

Decision Date2012-09-24
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BLOOD PRESSURE MONITOR WITH STETHOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Hangzhou Reli-On Co., Ltd.. It received FDA 510(k) clearance on 2012-09-24 under 510(k) number K122259. The device is classified under product code DXQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BLOOD PRESSURE MONITOR WITH STETHOSCOPE?

BLOOD PRESSURE MONITOR WITH STETHOSCOPE is a medical device that received FDA 510(k) clearance on 2012-09-24. The listed applicant is Hangzhou Reli-On Co., Ltd.. The 510(k) number is K122259.

When did BLOOD PRESSURE MONITOR WITH STETHOSCOPE receive FDA 510(k) clearance?

BLOOD PRESSURE MONITOR WITH STETHOSCOPE received FDA 510(k) clearance on 2012-09-24, under 510(k) number K122259.

Who is the listed applicant for BLOOD PRESSURE MONITOR WITH STETHOSCOPE?

The FDA 510(k) record lists Hangzhou Reli-On Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BLOOD PRESSURE MONITOR WITH STETHOSCOPE?

The FDA product code for BLOOD PRESSURE MONITOR WITH STETHOSCOPE is DXQ.

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.

Related Devices (Code: DXQ)

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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