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FDA 510(k)

KING`YIELD WRIST BLOOD PRESSURE MONITOR, MODEL BP201

K-Number: K083043 · 2008-10-27

Decision Date2008-10-27
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

KING`YIELD WRIST BLOOD PRESSURE MONITOR, MODEL BP201 is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Kingyield Technology Co., Ltd.. It received FDA 510(k) clearance on 2008-10-27 under 510(k) number K083043. 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 KING`YIELD WRIST BLOOD PRESSURE MONITOR, MODEL BP201?

KING`YIELD WRIST BLOOD PRESSURE MONITOR, MODEL BP201 is a medical device that received FDA 510(k) clearance on 2008-10-27. The listed applicant is Shenzhen Kingyield Technology Co., Ltd.. The 510(k) number is K083043.

When did KING`YIELD WRIST BLOOD PRESSURE MONITOR, MODEL BP201 receive FDA 510(k) clearance?

KING`YIELD WRIST BLOOD PRESSURE MONITOR, MODEL BP201 received FDA 510(k) clearance on 2008-10-27, under 510(k) number K083043.

Who is the listed applicant for KING`YIELD WRIST BLOOD PRESSURE MONITOR, MODEL BP201?

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

What is the FDA product code for KING`YIELD WRIST BLOOD PRESSURE MONITOR, MODEL BP201?

The FDA product code for KING`YIELD WRIST BLOOD PRESSURE MONITOR, MODEL BP201 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 Shenzhen Kingyield Technology 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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