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FDA 510(k)

TRICOT BLOOD PRESSURE CUFF

K-Number: K051539 · 2005-08-05

Decision Date2005-08-05
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TRICOT BLOOD PRESSURE CUFF is the device name listed in this FDA 510(k) record. The listed applicant is Ya Horng Electronic Co., Ltd.. It received FDA 510(k) clearance on 2005-08-05 under 510(k) number K051539. 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 TRICOT BLOOD PRESSURE CUFF?

TRICOT BLOOD PRESSURE CUFF is a medical device that received FDA 510(k) clearance on 2005-08-05. The listed applicant is Ya Horng Electronic Co., Ltd.. The 510(k) number is K051539.

When did TRICOT BLOOD PRESSURE CUFF receive FDA 510(k) clearance?

TRICOT BLOOD PRESSURE CUFF received FDA 510(k) clearance on 2005-08-05, under 510(k) number K051539.

Who is the listed applicant for TRICOT BLOOD PRESSURE CUFF?

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

What is the FDA product code for TRICOT BLOOD PRESSURE CUFF?

The FDA product code for TRICOT BLOOD PRESSURE CUFF 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.

Other records listing Ya Horng 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.

View all 10 devices →

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

View on FDA Database →

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

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