Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

BP 101 DIGITAL BLOOD PRESSURE MONITOR

K-Number: K062033 · 2007-03-23

Decision Date2007-03-23
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BP 101 DIGITAL BLOOD PRESSURE MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Kingyield Hongkong Limited. It received FDA 510(k) clearance on 2007-03-23 under 510(k) number K062033. 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 BP 101 DIGITAL BLOOD PRESSURE MONITOR?

BP 101 DIGITAL BLOOD PRESSURE MONITOR is a medical device that received FDA 510(k) clearance on 2007-03-23. The listed applicant is Kingyield Hongkong Limited. The 510(k) number is K062033.

When did BP 101 DIGITAL BLOOD PRESSURE MONITOR receive FDA 510(k) clearance?

BP 101 DIGITAL BLOOD PRESSURE MONITOR received FDA 510(k) clearance on 2007-03-23, under 510(k) number K062033.

Who is the listed applicant for BP 101 DIGITAL BLOOD PRESSURE MONITOR?

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

What is the FDA product code for BP 101 DIGITAL BLOOD PRESSURE MONITOR?

The FDA product code for BP 101 DIGITAL 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.

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑