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FDA 510(k)

YP-710T Series NIBP Cuff;YP-840T Series Disposable Cuff

K-Number: K260747 · 2026-05-06

Decision Date2026-05-06
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

YP-710T Series NIBP Cuff;YP-840T Series Disposable Cuff is the device name listed in this FDA 510(k) record. The listed applicant is Nihon Kohden Corporation. It received FDA 510(k) clearance on 2026-05-06 under 510(k) number K260747. 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 YP-710T Series NIBP Cuff;YP-840T Series Disposable Cuff?

YP-710T Series NIBP Cuff;YP-840T Series Disposable Cuff is a medical device that received FDA 510(k) clearance on 2026-05-06. The listed applicant is Nihon Kohden Corporation. The 510(k) number is K260747.

When did YP-710T Series NIBP Cuff;YP-840T Series Disposable Cuff receive FDA 510(k) clearance?

YP-710T Series NIBP Cuff;YP-840T Series Disposable Cuff received FDA 510(k) clearance on 2026-05-06, under 510(k) number K260747.

Who is the listed applicant for YP-710T Series NIBP Cuff;YP-840T Series Disposable Cuff?

The FDA 510(k) record lists Nihon Kohden Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for YP-710T Series NIBP Cuff;YP-840T Series Disposable Cuff?

The FDA product code for YP-710T Series NIBP Cuff;YP-840T Series Disposable Cuff is DXQ.

Other records listing Nihon Kohden Corporation 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 19 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.