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FDA 510(k)

DIGITAL BLOOD PRESSURE MONITOR, MODEL DS-181

K-Number: K993890 · 1999-12-01

ApplicantNihon Seimitsu Sokki Co., Ltd.
Decision Date1999-12-01
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DIGITAL BLOOD PRESSURE MONITOR, MODEL DS-181 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 1999-12-01 under 510(k) number K993890. 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 DIGITAL BLOOD PRESSURE MONITOR, MODEL DS-181?

DIGITAL BLOOD PRESSURE MONITOR, MODEL DS-181 is a medical device that received FDA 510(k) clearance on 1999-12-01. The listed applicant is Nihon Seimitsu Sokki Co., Ltd.. The 510(k) number is K993890.

When did DIGITAL BLOOD PRESSURE MONITOR, MODEL DS-181 receive FDA 510(k) clearance?

DIGITAL BLOOD PRESSURE MONITOR, MODEL DS-181 received FDA 510(k) clearance on 1999-12-01, under 510(k) number K993890.

Who is the listed applicant for DIGITAL BLOOD PRESSURE MONITOR, MODEL DS-181?

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 DIGITAL BLOOD PRESSURE MONITOR, MODEL DS-181?

The FDA product code for DIGITAL BLOOD PRESSURE MONITOR, MODEL DS-181 is DXN.

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Other records listing Nihon Seimitsu Sokki Co., Ltd. as applicant

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Related Devices (Code: DXN)

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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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