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FDA 510(k)

BLOOD PRESSURE MONITOR (SPHYGMOMANOMETER), MODEL HT-110

K-Number: K012194 · 2001-07-20

Decision Date2001-07-20
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BLOOD PRESSURE MONITOR (SPHYGMOMANOMETER), MODEL HT-110 is the device name listed in this FDA 510(k) record. The listed applicant is Nihon Seimitsu Sokki Co., Ltd.. It received FDA 510(k) clearance on 2001-07-20 under 510(k) number K012194. 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 BLOOD PRESSURE MONITOR (SPHYGMOMANOMETER), MODEL HT-110?

BLOOD PRESSURE MONITOR (SPHYGMOMANOMETER), MODEL HT-110 is a medical device that received FDA 510(k) clearance on 2001-07-20. The listed applicant is Nihon Seimitsu Sokki Co., Ltd.. The 510(k) number is K012194.

When did BLOOD PRESSURE MONITOR (SPHYGMOMANOMETER), MODEL HT-110 receive FDA 510(k) clearance?

BLOOD PRESSURE MONITOR (SPHYGMOMANOMETER), MODEL HT-110 received FDA 510(k) clearance on 2001-07-20, under 510(k) number K012194.

Who is the listed applicant for BLOOD PRESSURE MONITOR (SPHYGMOMANOMETER), MODEL HT-110?

The FDA 510(k) record lists Nihon Seimitsu Sokki Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BLOOD PRESSURE MONITOR (SPHYGMOMANOMETER), MODEL HT-110?

The FDA product code for BLOOD PRESSURE MONITOR (SPHYGMOMANOMETER), MODEL HT-110 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 Nihon Seimitsu Sokki 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 21 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

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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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