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FDA 510(k)

KD-622 FULLY AUTOMATIC ELECTRONIC BLOOD PRESSURE MONITOR

K-Number: K030358 · 2003-10-31

Decision Date2003-10-31
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

KD-622 FULLY AUTOMATIC ELECTRONIC BLOOD PRESSURE MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Kodon(Tianjin)Electronic&Electrical Apparatus Co.,. It received FDA 510(k) clearance on 2003-10-31 under 510(k) number K030358. 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 KD-622 FULLY AUTOMATIC ELECTRONIC BLOOD PRESSURE MONITOR?

KD-622 FULLY AUTOMATIC ELECTRONIC BLOOD PRESSURE MONITOR is a medical device that received FDA 510(k) clearance on 2003-10-31. The listed applicant is Kodon(Tianjin)Electronic&Electrical Apparatus Co.,. The 510(k) number is K030358.

When did KD-622 FULLY AUTOMATIC ELECTRONIC BLOOD PRESSURE MONITOR receive FDA 510(k) clearance?

KD-622 FULLY AUTOMATIC ELECTRONIC BLOOD PRESSURE MONITOR received FDA 510(k) clearance on 2003-10-31, under 510(k) number K030358.

Who is the listed applicant for KD-622 FULLY AUTOMATIC ELECTRONIC BLOOD PRESSURE MONITOR?

The FDA 510(k) record lists Kodon(Tianjin)Electronic&Electrical Apparatus Co., as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KD-622 FULLY AUTOMATIC ELECTRONIC BLOOD PRESSURE MONITOR?

The FDA product code for KD-622 FULLY AUTOMATIC 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 Kodon(Tianjin)Electronic&Electrical Apparatus Co., 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.

View all 9 devices →

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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